DOCSLIB.ORG

Subject Index

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Subject Index SUBJECT INDEX SUBJECT INDEX Abbe flap, vermilion submucosal pedicle, for upper lip Accurate platelet counts for platelet rich plasma, validation reconstruction (Special Section: Cancer), 17:1259– of hematology analyzer and preparation techniques 1262 for counting and (Scientific Foundation), 16:749– Abbé island flap (Original Articles), 18:766–768 759 Abducens nerve, microanatomic and endoscopic study Acellular cadaveric dermis, experimental study of (Scientific (Literature Scan), 19:546 Foundations), 18:551–558 Abortive subtype of frontoethmoidal encephalocele (Case Acellular human dermis (alloderm), exposed skull with, one- Report), 10:149–154 stage skin grafting of (Technical Experience), Abraxane, for treatment of metastatic breast cancer (Special 19:1660–1662 Editorial), 17:3–7 Acetylic resin, in conjunction with silicon for maxillofacial Abrikossoff’s tumor (Clinical Note), 12:78–81 rehabilitation (Brief Clinical Notes), 17:152–162 Abscess, brain, from cranio-orbital foreign body (Clinical Achondroplasia and Pfeiffer syndrome, genetic relationship Note), 7:311–314 between (Clinical Note), 9:477–480 Absent ear, bone-anchored implants for (Scientific Acoustic evoked potentials in neurophysiological Foundation), 19:744–747 evaluation in craniostenosis and craniofacial Absorbable. See also under Bioabsorbable stenosis, 8:286–289 Absorbable biomaterial in craniofacial skeleton fixation, Acquired orbital deformity, reconstruction of (Clinical 10:491 Note), 19:1092–1097 Absorbable fixation Acrocephalosyndactyly, 7:23–30, 8:279–283 for craniomaxillofacial surgery (Clinical Note), 11:575 fibroblast growth factor receptor 2 gene mutations and internal, critical concepts of (Scientific Foundation), (Scientific Foundation), 9:162–170 11:335–341 in Pfeiffer’s syndrome (Clinical Report), 9:83–87 in zygomaticomaxillary fracture repair (Clinical Note), in syndromic craniosynostosis, 9:201–205 11:377–385 Acrocephalosyndactyly syndrome (Clinical Note), 11:480– Absorbable osteofixation devices, naturally (Overview 486 Section), 14:247–259 Acromegalic face, surgical management of (Clinical Note), Absorbable plates, and Mimix, in reconstruction of cranial 5:336 bone defects (Scientific Foundation), 19:1131– Acrylic cranioplasty (Literature Scan), 9:303 1135 Acrylic resin, in conjunction with silicon for maxillofacial Absorbable plating rehabilitation (Brief Clinical Notes), 17:152–162 early failure of, in a patient with syndromic Acrylic skull replica, computer-generated, produced by laser brachycephaly (Clinical Notes), 15:519–522 lithography, 9:222–226 Discussion, 15:522 Actinomycosis of masseter muscle: report of case and review polylactic acid, skull defect utilizing, and carbonated of literature (Clinical Note), 14:915–918 apatite bone cement, new method of pediatric parotid gland combined with, false diagnosis cranioplasty for (Technical Strategies), 15:469– caused by Warthin tumor (Clinical Notes), 472 14:46–50 Absorbable plating for fixation, 7:325 Acute bacterial suppurative parotitis: microbiology and Absorbable rigid fixation management (Clinical Notes), 14:37–40 of craniofacial skeleton, system applications for Adams-Oliver syndrome, aplasia cutis in, surgery for, (Technical Strategy), 7:394–398 12:569–572 in growing skull fracture repair, 9:65–73 Adaptive therapy for cleft palate patient (Clinical Note), Acanthosis nigrans in Crouzon’s disease, 5:220 11:66–70 ACC. See Adenoid cystic carcinoma (ACC) Adenoid cystic carcinoma (ACC), nasal, with intracranial Accessory auricula extension (Brief Clinical Notes), 17:1026–1029 cervical (Brief Clinical Notes), 17:713–715 Adenoid cystic carcinoma, neurotrophic spread of, in goldenhar syndrome presenting with (Clinical Notes), maxillofacial district, pre- and postsurgical 17:669–672 adjuvant treatment of (Brief Clinical Notes), Accessory parotid gland tumors 16:332–334 cavernous vascular tumor of (Brief Clinical Notes), Adenoid cystic carcinoma (ACC), of parotid gland, after superficial parotidectomy for benign lesion (Brief 18:1493–1496 Clinical Notes), 18:231–235 resection through peroral approach with facial nerve Adenoma, pleomorphic, of parotid gland, surgery for, monitoring (Technical Experiences), 18:1419– 12:565–568 1421 Adenoma, pituitary, transnasal transseptal endoscopic Accessory pituitary gland, infantile hemangioma of (Clinical approach to, 8:159–163 Note), 9:468–471 1 THE JOURNAL OF CRANIOFACIAL SURGERY Adenoma, pleomorphic, surgical removal of (Brief Clinical Aesthetic balance, restoration of, with mandibular surgery, Notes), 17:1001–1004 for missing maxilla, 2:95–100 Adhesives, use of, in cleft palate surgery, new flap fixation Aesthetic improvement, new modified forked flap with technique and (Brief Clinical Notes), 16:719–722 subcutaneous pedicles for bilateral cleft lip nasal Adipose-derived stem cells (ASCs), rabbit, isolation and deformity (Technical Strategy), 19:1374–1380 osteoblastic differentiation of, 19:360–368 Aesthetic surgery, state of art procedure of rhinoplasty in Adipose-derived stromal cells (ASCs) (Original Article), 19:1491–1496 neurospheres from, as neural progenitors in vitro and in Afghanistan, and Iraq, trauma caused by conflicts in, vivo (Scientific Foundations), 18:49–53 reflections on (Special Editorial), 19:297–299 used in autologous fashion tissue regeneration (Original African American 3D CT skull images, 9:348–358 Articles), 18:789–790 commentary on, 9:359 Adipose precursor cells (APCs), leporine-derived, Age exhibition of in vitro osteogenic potential in, complications of craniofacial surgery and, 8:345 19:360–368 demineralized bone donation and (Scientific Adipose tissue, tumor of, hibernoma as (Clinical Note), Foundation), 9:142–146 12:284–286 Age, parietal bone thickness and, 11:17–23 Adjuvant radiotherapy Agenesis, parietal bone, and associated multiple congenital of basal cell carcinomas (BCC) and squamous cell anomalies (Clinical Notes), 14:192–196 carcinomas (SCC), criteria for, (Original Agenesis, premaxilla, intraoral distraction of patient with Articles), 18:1024 (Brief Clinical Notes), 16:500–503 postoperative, for kimura disease (Clinical Notes), Aggressiveness of microcystic adnexal carcinoma (Clinical 18:1062–1066 Notes), 16:53–58 Administrators (Editorial), 11:73–74 Aging, effect on thickness of upper eyelid (Anatomic Adnexal carcinoma, microcystic, misdiagnosis and Studies), 17:474–476 aggressiveness of (Clinical Notes), 16:53–58 Aging face syndrome, total facial rehabilitation for, 8:194– Adolescence, severe maxillary deficiency in, distraction 199 osteogenesis for, 8:181–186 Airway Adolescent population, bilateral reduction mammoplasty in: changes in, after Le Fort III osteotomy in adolescent bilateral reduction mammoplasty, craniosynostosis syndromes (Clinical Note), 14:691–695 7:363–369 Adolescents, mixed odontogenic tumors in (Clinical Notes), in craniosynostosis, assessment of, 2:162A 18:1338–1342 laryngeal mask, nasolaryngeal ventilation with, in Adopted child management in craniofacial clinic, 6:143– dental surgery (Clinical Note), 9:383–387 146 management of, operative, for midface fractures, Adult survey of, 8:201–206 with anteroposterior skeletal disharmony, cranial base nasal, effect of maxillary expansion on (Clinical Notes), flexion of, 19:334–338 17:1045–1049 bone healing in presence of implantable fixation devices obstruction of, in Treacher-Collins syndrome, in (Editorial), 19:1435–1437 mandibular lengthening by distraction for, Crouzon disease in, modified Le Fort III osteotomy in 5:22–25 commentary on, 9:486–487 Airway management (Technical Strategy), 9:481–485 of Pfeiffer syndrome patients with tracheal cartilaginous Adult orthognathic surgery, (Orthognathic Surgery sleeve and cricoid cartilage involvement during Continued), 18:1197–1208 surgical tracheostomy (Clinical Notes), Adult patients, after otoplasty, HRQOL outcome of 17:272–274 (Original Articles), 17:629–635 in PRS, subperiosteal release of floor of the mouth in, Advanced Trauma Life Support Manual, on association of 19:609–615 cervical spine fractures with maxillofacial trauma Airway obstruction, in micrognathic infants, mandibular (Original Article), 18:1259–1263 distraction with internal curvilinear device Advancement, mallar augmentation by (Technical Strategy), (Technical Experiences), 18:1403–1407 4:257–264 Airway obstruction, upper, correction of, in newborn with Advancement osteotomy, Le Fort III, in growing child internal mandibular distraction osteogenesis affected by Crouzon’s and Apert’s syndromes, (Technical Strategy), 14:493–499 presurgical and postsurgical growth and (Clinical Airway in severe mandibular hypoplasia, treatment and Notes), 16:369–377 (Clinical Note), 12:337–348 Aerodynamics, speech, and nasalance in oral cancer patients Airway space, pharyngeal, changes in, after body treated with microvascular transfers (Clinical ostectomies and sagittal split ramus osteotomies Studies), 16:990–996 (Clinical Study), 16:23–30 2 SUBJECT INDEX Ala, morphofunctional reconstruction of (Brief Clinical Alloplastic PMMA cranioplasty materials, biomechanical Notes), 18:1475–1479 testing of (Technical Strategies), 16:140–143 Ala nasi, triangular (TAN) repair of unilateral cleft lips Alloplastic prosthesis in temporomandibular joint (Technical Strategies), 18:186–197 reconstruction, 3:160–169 Alar cinch suture in Le Fort I osteotomy (Technical Alloplastic stabilization, microscrew anchorage techniques Strategy), 7:399–402 for, 2:72–73 Alar cleft, Tessier 1, congenital isolated, reconstruction of Alloplastic tumor of palate (Images From
Load more

Recommended publications
  • Glossary for Narrative Writing
    Periodontal Assessment and Treatment Planning Gingival description Color: o pink o erythematous o cyanotic o racial pigmentation o metallic pigmentation o uniformity Contour: o recession o clefts o enlarged papillae o cratered papillae o blunted papillae o highly rolled o bulbous o knife-edged o scalloped o stippled Consistency: o firm o edematous o hyperplastic o fibrotic Band of gingiva: o amount o quality o location o treatability Bleeding tendency: o sulcus base, lining o gingival margins Suppuration Sinus tract formation Pocket depths Pseudopockets Frena Pain Other pathology Dental Description Defective restorations: o overhangs o open contacts o poor contours Fractured cusps 1 ww.links2success.biz [email protected] 914-303-6464 Caries Deposits: o Type . plaque . calculus . stain . matera alba o Location . supragingival . subgingival o Severity . mild . moderate . severe Wear facets Percussion sensitivity Tooth vitality Attrition, erosion, abrasion Occlusal plane level Occlusion findings Furcations Mobility Fremitus Radiographic findings Film dates Crown:root ratio Amount of bone loss o horizontal; vertical o localized; generalized Root length and shape Overhangs Bulbous crowns Fenestrations Dehiscences Tooth resorption Retained root tips Impacted teeth Root proximities Tilted teeth Radiolucencies/opacities Etiologic factors Local: o plaque o calculus o overhangs 2 ww.links2success.biz [email protected] 914-303-6464 o orthodontic apparatus o open margins o open contacts o improper
    [Show full text]
  • Soonerstart Automatic Qualifying Syndromes and Conditions 001
    SoonerStart Automatic Qualifying Syndromes and Conditions 001 Abetalipoproteinemia 272.5 002 Acanthocytosis (see Abetalipoproteinemia) 272.5 003 Accutane, Fetal Effects of (see Fetal Retinoid Syndrome) 760.79 004 Acidemia, 2-Oxoglutaric 276.2 005 Acidemia, Glutaric I 277.8 006 Acidemia, Isovaleric 277.8 007 Acidemia, Methylmalonic 277.8 008 Acidemia, Propionic 277.8 009 Aciduria, 3-Methylglutaconic Type II 277.8 010 Aciduria, Argininosuccinic 270.6 011 Acoustic-Cervico-Oculo Syndrome (see Cervico-Oculo-Acoustic Syndrome) 759.89 012 Acrocephalopolysyndactyly Type II 759.89 013 Acrocephalosyndactyly Type I 755.55 014 Acrodysostosis 759.89 015 Acrofacial Dysostosis, Nager Type 756.0 016 Adams-Oliver Syndrome (see Limb and Scalp Defects, Adams-Oliver Type) 759.89 017 Adrenoleukodystrophy, Neonatal (see Cerebro-Hepato-Renal Syndrome) 759.89 018 Aglossia Congenita (see Hypoglossia-Hypodactylia) 759.89 019 Albinism, Ocular (includes Autosomal Recessive Type) 759.89 020 Albinism, Oculocutaneous, Brown Type (Type IV) 759.89 021 Albinism, Oculocutaneous, Tyrosinase Negative (Type IA) 759.89 022 Albinism, Oculocutaneous, Tyrosinase Positive (Type II) 759.89 023 Albinism, Oculocutaneous, Yellow Mutant (Type IB) 759.89 024 Albinism-Black Locks-Deafness 759.89 025 Albright Hereditary Osteodystrophy (see Parathyroid Hormone Resistance) 759.89 026 Alexander Disease 759.89 027 Alopecia - Mental Retardation 759.89 028 Alpers Disease 759.89 029 Alpha 1,4 - Glucosidase Deficiency (see Glycogenosis, Type IIA) 271.0 030 Alpha-L-Fucosidase Deficiency (see Fucosidosis)
    [Show full text]
  • Oral Diagnosis: the Clinician's Guide
    Wright An imprint of Elsevier Science Limited Robert Stevenson House, 1-3 Baxter's Place, Leith Walk, Edinburgh EH I 3AF First published :WOO Reprinted 2002. 238 7X69. fax: (+ 1) 215 238 2239, e-mail: [email protected]. You may also complete your request on-line via the Elsevier Science homepage (http://www.elsevier.com). by selecting'Customer Support' and then 'Obtaining Permissions·. British Library Cataloguing in Publication Data A catalogue record for this book is available from the British Library Library of Congress Cataloging in Publication Data A catalog record for this book is available from the Library of Congress ISBN 0 7236 1040 I _ your source for books. journals and multimedia in the health sciences www.elsevierhealth.com Composition by Scribe Design, Gillingham, Kent Printed and bound in China Contents Preface vii Acknowledgements ix 1 The challenge of diagnosis 1 2 The history 4 3 Examination 11 4 Diagnostic tests 33 5 Pain of dental origin 71 6 Pain of non-dental origin 99 7 Trauma 124 8 Infection 140 9 Cysts 160 10 Ulcers 185 11 White patches 210 12 Bumps, lumps and swellings 226 13 Oral changes in systemic disease 263 14 Oral consequences of medication 290 Index 299 Preface The foundation of any form of successful treatment is accurate diagnosis. Though scientifically based, dentistry is also an art. This is evident in the provision of operative dental care and also in the diagnosis of oral and dental diseases. While diagnostic skills will be developed and enhanced by experience, it is essential that every prospective dentist is taught how to develop a structured and comprehensive approach to oral diagnosis.
    [Show full text]
  • A Single Case Report of Granular Cell Tumor of the Tongue Successfully Treated Through 445 Nm Diode Laser
    healthcare Case Report A Single Case Report of Granular Cell Tumor of the Tongue Successfully Treated through 445 nm Diode Laser Maria Vittoria Viani 1,*, Luigi Corcione 1, Chiara Di Blasio 2, Ronell Bologna-Molina 3 , Paolo Vescovi 1 and Marco Meleti 1 1 Department of Medicine and Surgery, University of Parma, 43126 Parma, Italy; [email protected] (L.C.); [email protected] (P.V.); [email protected] (M.M.) 2 Private practice, Centro Medico Di Blasio, 43121 Parma; Italy; [email protected] 3 Faculty of Dentistry, University of the Republic, 14600 Montevideo, Uruguay; [email protected] * Correspondence: [email protected] Received: 10 June 2020; Accepted: 11 August 2020; Published: 13 August 2020 Abstract: Oral granular cell tumor (GCT) is a relatively rare, benign lesion that can easily be misdiagnosed. Particularly, the presence of pseudoepitheliomatous hyperplasia might, in some cases, lead to the hypothesis of squamous cell carcinoma. Surgical excision is the treatment of choice. Recurrence has been reported in up to 15% of cases treated with conventional surgery. Here, we reported a case of GCT of the tongue in a young female patient, which was successfully treated through 445 nm diode laser excision. Laser surgery might reduce bleeding and postoperative pain and may be associated with more rapid healing. Particularly, the vaporization effect on remnant tissues could eliminate GCT cells on the surgical bed, thus hypothetically leading to a lower rate of recurrence. In the present case, complete healing occurred in 1 week, and no recurrence was observed after 6 months. Laser surgery also allows the possibility to obtain second intention healing.
    [Show full text]
  • Congenital Epulis: Unusual Etiology of Airway Obstruction and Feeding Failure in a Newborn Shilpa Vishwanath, MD,MS1; H
    Congenital Epulis: Unusual Etiology of Airway Obstruction and Feeding Failure in a Newborn Shilpa Vishwanath, MD,MS1; H. James Williams, MD2; Aaron C. Mason, MD3 1West Virginia University Department of Otolaryngology, Morgantown WV; 2Department of Pathology, West Virginia University 3Division of Plastic, Reconstructive, and Hand Surgery, West Virginia University Abstract Title: Congenital Epulis: Unusual Etiology of Airway Obstruction and Feeding Failure in a Newborn Objectives: Review congenital epulis; Its presentation and management. Study Design: Case Report Methods: Description of a newborn presenting with an obstructing oral mass. A review of the literature is included. Results: Congenital epulis is a rare oral lesion that may result in airway obstruction and/or feeding failure bringing the mass to the attention of subspecialists. Conclusion: A congenital epulis may present as a solitary alveolar mass in Figure 1 the newborn. Females are affected more often than males. Airway Results obstruction and feeding failure may evolve depending upon the size and The pathological specimen was a maxillary congenital granular cell tumor location of the lesion. Physical examination, radiographic evaluation, and (congenital epulis). pathologic review are useful in its evaluation and diagnosis. Pathology slides (Figure 3): Histopathologically, special stains assist in the differentiation of the lesion (A) H&E stain, 4x: There is a subepithelial proliferation of cells with from other solid tumors. Early intervention relieves airway obstruction and abundant eosinophilic cytoplasm. Note the absence of hyperplasia of the enables feeding success. overlying squamous epithelium and the prominence of vascular structures. (B) H&E stain, 20x: The tumor cells have abundant granular cytoplasm (low N/C ratio) and small uniform nuclei.
    [Show full text]
  • Physician Service Fee Schedule-Affordable Care Act(ACA) Taxonomy Defined Rates Pricing Specialty 01E Fee Schedule Updated On: 6/26/2020
    NC Medicaid Physician Services Fee Schedule (See Affordable Care Act (ACA) Tab for Applicable ACA Defined Taxonomy Rates) Provider Specialty 001 Fee Schedule Updated on: 6/26/2020 ***The Agency's fee schedule rates below were set as of January 1, 2014 unless otherwise noted*** Rate changes after January 1, 2014 are based on the January 1st RVU of the year in which the service was initally established. The inclusion of a rate on this table does not guarantee that a service is covered. Please refer to the Medicaid Billing Guide and the Medicaid and Health Choice Clinical Policies on the DHB Web Site. Providers should always bill their usual and customary charges. Please use the monthly NC Medicaid Bulletins for additions, changes and deletion to this schedule. Medicaid Maximum Allowable NON-FACILITY Effective FEE END DATE PROCEDURE CODE MODIFIER PROCEDURE DESCRIPTION FACILITY RATE RATE Date of Rate 01967 ANESTH/ANALG VAG DELIVERY $ 220.11 $ 220.11 3/1/2020 12/31/9999 01996 HOSP MANAGE CONT DRUG ADMIN $ 40.88 $ 40.88 3/1/2020 12/31/9999 10004 FNA BX W/O IMG GDN EA ADDL $ 38.83 $ 46.10 3/1/2020 12/31/9999 10005 FNA BX W/US GDN 1ST LES $ 65.75 $ 110.89 3/1/2020 12/31/9999 10006 FNA BX W/US GDN EA ADDL $ 44.80 $ 53.29 3/1/2020 12/31/9999 10007 FNA BX W/FLUOR GDN 1ST LES $ 84.41 $ 247.72 3/1/2020 12/31/9999 10008 FNA BX W/FLUOR GDN EA ADDL $ 55.05 $ 139.88 3/1/2020 12/31/9999 10009 FNA BX W/CT GDN 1ST LES $ 102.46 $ 404.53 3/1/2020 12/31/9999 10010 FNA BX W/CT GDN EA ADDL $ 74.89 $ 244.25 3/1/2020 12/31/9999 10011 FNA BX W/MR GDN 1ST LES $ 54.57
    [Show full text]
  • A Study of Incidence of Congenital Cardiac Anomalies in the New- Borns with Ano-Rectal Malformation: Our Hospital Experience
    Original Research Article Indian Journal of Anesthesia and Analgesia1973 2018; 5(12): 1973­76 DOI: http://dx.doi.org/10.21088/ijaa.2349.8471.51218.1 A Study of Incidence of Congenital Cardiac Anomalies in the New- Borns with Ano-Rectal Malformation: Our Hospital Experience Y.V.S. Ravi Nagaprasad1, Aavula Muralidhar2 1,2Associate Professor, Department of Anesthesiology, Niloufer Hospital for Women and Child, Osmania Medical Collage, Hyderabad, Telangana 500095, India. Abstract Background: Ano­rectal malformation is a common anomaly seen in newborns and is associated with multiple anomalies like renal, vertebral, muscular and cardiac. Associated cardiac anomalies determine the morbidity and mortality of newborn. It is mandatory to properly evaluate the child for cardiac anomalies in children with ARM. Objective: The aim of the study is to evaluate the incidence of associated cardiac anomalies in thenew­borns with Ano­rectal malformation admitted ina tertiary care centre. Method: Total number of Ano­rectal Malformation admitted from June 2017 to May 2018 in our hospital was recorded. All cases after examination and evaluation were classified into Low ARM and High ARM. All cases after preoperative evaluations and basic haematological tests were taken for emergency colostomy or cut back anoplasty. Patients during postoperative period were performed echocardiogram for cardiac evaluation. Total number newborns with ARM having associated cardiac anomalies were determined. The incidence of cardiac anomalies in two types of ARM was determined. Results: Total number of newborns with ARM admitted for sugery in the period of June 2017 to May 2018 were 182. Out of which 21 cases were having congenital cardiac anomalies (11.53%).
    [Show full text]
  • A Study on Etiology and Incidence of Formation of Types of Anorectal Malformation
    International Journal of Surgery Science 2019; 3(4): 100-103 E-ISSN: 2616-3470 P-ISSN: 2616-3462 © Surgery Science A study on Etiology and incidence of formation of types www.surgeryscience.com 2019; 3(4): 100-103 of Anorectal malformation: A prospective study Received: 18-08-2019 Accepted: 22-09-2019 Dr. Mohd Zakir Mohiuddin Owais, Dr. T Vinodh Kumar, Dr. Hasanthi, Dr. Mohd Zakir Mohiuddin Owais Assistant Professor, Department of R Suman and A Madhu Paediatric Surgery, Niloufer Hospital, Hyderabad, Telangana, DOI: https://doi.org/10.33545/surgery.2019.v3.i4b.225 India Abstract Dr. T Vinodh Kumar Background: Anorectal malformations are one of the most common congenital defects. This study was Assistant Professor, Department of undertaken to study the hospital incidence of anorectal malformations (ARM), frequency of various types Paediatric Surgery, Sri Venkateswara Medical College, of defects, their sex distribution and the spectrum of anomalies associated with ARM. Tirupati, Andhra Pradesh, India Materials and Methods: Ninety consecutive children attending the paediatric surgery department were included in this study. A detailed history was taken, and examination was performed for the primary as Dr. Hasanthi well as the associated defects. Appropriate investigations like invertogram, cologram were done wherever Assistant Professor, Department of indicated. Management was as per the standard protocol. The data was recorded and analyzed. Paediatric Surgery, Guntur Results: Out of the 90 patients, 52(57.77%) male patients and 38(42.22%) female patients. Most of our Medical College & Govt General patients presented within first 24 hours of life. Patients who presented after 72 hours were either female Hospital, Guntur, Andhra Pradesh, patients with anovestibular malformation or male patients with anocutaneous fistula.
    [Show full text]
  • Orthotic Management of Pt's With
    David B. Misener, B.Sc.(H.K.), CPO, MBA ABC Certified Orthotist & Prosthetist CMTa Advisory Board Member Clinical Prosthetics & Orthotics, LLC, Albany, NY CMT 1B Contributors: Ken Cornell, CO, FAAOP Cornell O&P, Peabody, MA S Sean McCale, CO Midwest Orthotic & Technology Center, Chicago, IL Point of view from Orthotist S Description of CMT S Some History S Understand the disease process S Pathophysiology S Pathomechanics S Critical insight into best designs S Patient Evaluation S Orthotic Management Options History 1886 2 papers were submitted Howard Henry Tooth Cambridge Thesis: “The Peroneal type of Jean-Martin Charcot Progressive Muscular Atrophy” 61 y/o 29 y/o Pierre Marie 33 y/o S Other names: Peroneal Muscular Atrophy, HMSN: Hereditary Motor Sensory Neuropathy, Charcot-Marie-Tooth-Hoffman, Tooth’s Motor sensory neuropathy S Description: A progressive inherited neuropathy that is characterized by motor and sensory loss, predominantly in the feet and legs but also in the hands and arms. Proportion of CMT S CMT1 Demyelination S CMT2 Axonal degeneration S Currently there are ~ 80 different kinds of CMT EMG Studies Demyelinating Axonal Degeneration S peripheral neuropathy characterized by: S Chronic denervation on EMG in distal muscles with S Slow nerve conduction velocity typically 5-30 meters per second; S Reduced compound motor action potentials S Normal CV S Normal action potentials S Tibial nerve 47.8 m/s S Tibial nerve 8.8 mV S Peroneal nerve 47.1 m/s S Peroneal nerve 6.0 mV S Hypertrophic peripheral nerves with onion S Near-normal
    [Show full text]
  • On the Inheritance of Hand and Foot Anomalies in Six Families
    On the Inheritance of Hand and Foot Anomalies in Six Families OLA JOHNSTON AND RALPH WALDO DAVIS Department of Biology, North Texas State College, Denton, Texas INTRODUCTION Malformations of the hands and feet are common and of many kinds. Ac- cording to Gates (1946) there probably are more abnormalities of the hands and feet than of any other part of the body, with the exception of the eye. It is true that some hand and foot anomalies are the result of accident and disease but it is equally true that many are the result of variation in heredity. The extent to which the latter is true and the mode of inheritance of those variations which have some genetic basis are questions which are not com- pletely answered. Hence when an opportunity presented itself to study a number of different hand and foot anomalies which appeared to have a he- reditary basis, it seemed worthwhile to investigate them and to present the findings. The malformations which are included are syndactyly and split hand and foot, polydactyly, and brachydactyly. Each will be considered more or less independently and in the order indicated. A BRIEF REVIEW OF LITERATURE 1. Syndactyly and Split Hand and Foot Syndactyly is the condition in which two or more fingers or toes are adherent or are more or less completely grown together. Split hand and foot (also called lobster claw) is a deformity in which the central digits of the hands and/or feet are lacking. It may represent an extreme variant of syndactyly. According to Lewis (1909) a description of split hand and foot is difficult because of the great variation in the deformity even within the same family.
    [Show full text]
  • Treatments for Ankyloglossia and Ankyloglossia with Concomitant Lip-Tie Comparative Effectiveness Review Number 149
    Comparative Effectiveness Review Number 149 Treatments for Ankyloglossia and Ankyloglossia With Concomitant Lip-Tie Comparative Effectiveness Review Number 149 Treatments for Ankyloglossia and Ankyloglossia With Concomitant Lip-Tie Prepared for: Agency for Healthcare Research and Quality U.S. Department of Health and Human Services 540 Gaither Road Rockville, MD 20850 www.ahrq.gov Contract No. 290-2012-00009-I Prepared by: Vanderbilt Evidence-based Practice Center Nashville, TN Investigators: David O. Francis, M.D., M.S. Sivakumar Chinnadurai, M.D., M.P.H. Anna Morad, M.D. Richard A. Epstein, Ph.D., M.P.H. Sahar Kohanim, M.D. Shanthi Krishnaswami, M.B.B.S., M.P.H. Nila A. Sathe, M.A., M.L.I.S. Melissa L. McPheeters, Ph.D., M.P.H. AHRQ Publication No. 15-EHC011-EF May 2015 This report is based on research conducted by the Vanderbilt Evidence-based Practice Center (EPC) under contract to the Agency for Healthcare Research and Quality (AHRQ), Rockville, MD (Contract No. 290-2012-00009-I). The findings and conclusions in this document are those of the authors, who are responsible for its contents; the findings and conclusions do not necessarily represent the views of AHRQ. Therefore, no statement in this report should be construed as an official position of AHRQ or of the U.S. Department of Health and Human Services. The information in this report is intended to help health care decisionmakers—patients and clinicians, health system leaders, and policymakers, among others—make well-informed decisions and thereby improve the quality of health care services. This report is not intended to be a substitute for the application of clinical judgment.
    [Show full text]
  • Anorectal Malformations
    Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine 1065 Anorectal Malformations Long-term outcome and aspects of secondary treatment JOHAN DANIELSON ACTA UNIVERSITATIS UPSALIENSIS ISSN 1651-6206 ISBN 978-91-554-9140-6 UPPSALA urn:nbn:se:uu:diva-241243 2015 Dissertation presented at Uppsala University to be publicly examined in Rosénsalen, Entrance 95/96, ground floor, Uppsala University Children’s Hospital, Uppsala, Friday, 27 February 2015 at 13:15 for the degree of Doctor of Philosophy (Faculty of Medicine). The examination will be conducted in English. Faculty examiner: Adjungerad Professor Olof Hallböök (Linköpings universitet ). Abstract Danielson, J. 2015. Anorectal Malformations. Long-term outcome and aspects of secondary treatment. Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine 1065. 109 pp. Uppsala: Acta Universitatis Upsaliensis. ISBN 978-91-554-9140-6. Faecal incontinence (FI) is defined as the inability to control bowel movements. The causes of FI are many and diverse. One of the more uncommon reasons for FI is Anorectal Malformations (ARMs). An ARM is a congenital anomaly that affects somewhere between 1/2500 and 1/5000 live born babies. Many ARM patients have persistent FI. Several different procedures have been utilised to address this issue. This thesis aims to evaluate (1) the long-term outcome in adulthood of ARMs in relation to the modern Krickenbeck classification, and (2) scope for treating FI with transanal injection with dextranomer in non-animal stabilised hyaluronic acid (NASHA/Dx), in patients both with and without ARMs. All patients treated for ARMs in Uppsala up to 1993 were invited to participate in a questionnaire study of quality of life and function.
    [Show full text]