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Oculo-auditory syndromes

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Published by Masson Pub. USA in New York .
Written in English

Subjects:

  • Ear -- Diseases -- Diagnosis.,
  • Eye -- Diseases -- Diagnosis.,
  • Syndromes.,
  • Eye Diseases.,
  • Ear Diseases.,
  • Hearing Disorders.,
  • Vision Disorders.

Book details:

Edition Notes

Includes bibliographies and index.

StatementLucian S. Regenbogen, Gabriel J. Coscas.
ContributionsCoscas, Gabriel.
Classifications
LC ClassificationsRF123 R39 1985
The Physical Object
Paginationxi, 347 p. :
Number of Pages347
ID Numbers
Open LibraryOL2851974M
ISBN 100893522252
LC Control Number84014328

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Additional Physical Format: Online version: Regenbogen, Lucian S. Oculo-auditory syndromes. New York: Masson Pub. USA, © (OCoLC) Document Type. This book presents thorough, wellwritten, and interesting accounts of 70 syndromes with ocular and auditory manifestations. Some of the syndromes, such as the Small syndrome and the Sylvester syndrome, are rare. Many others, such as Crouzon's syn. Oculo-Auditory Syndromes / Lucian S. Regenbogen (Editor) / Neonatal Medicine / Leo Stern (Editor) / Nephrology / M. Legrain / Athenian Odyssey; A Unique Guide to Experiencing Ancient Athens / William Merle Taylor / Earth Science / James A. Woodhead / Oculo-auditory syndromes Lucian S. Regenbogen, Gabriel J. Coscas Masson Pub. USA, c

1. Author(s): Regenbogen,Lucian S; Coscas,Gabriel Title(s): Oculo-auditory syndromes/ Lucian S. Regenbogen, Gabriel J. Coscas. Country of Publication: United States.   Oculo-auditory syndromes have been reviewed by Regenbogen and Coscas, although not all the syndromes summarised by these authors cause deaf–blindness. Regenbogen and Godel [15] found ocular anomalies that were interfering with vision in 45% of the by: International Symposium on Inner Ear Therapies (ISIET), Marrakech, Morocco - 1. November 1. st, WELCOME. am. Request PDF | On Oct 1, , Birgit Herppich and others published Book Review: Roots and Remedies of the Dependency Syndrome in World Missions | Find, read and cite all the research you need on.

The facio-oculo-acoustico-renal syndrome (FOAR) is a rare autosomal recessive syndrome characterized by the presence of dysmorphic facial features, ocular . This book is scientific and practical as it provides the reader with a reasonable body of easily accessible knowledge that will allow each practitioner to understand, interpret, and adapt treatment in their patient's best interests.   Abstract Faciooculoacousticorenal (FOAR) syndrome [Donnai-Barrow syndrome; DBS/FOAR] is a rare autosomal recessive familial disorder that has resulted from mutations that have occurred on chromosome 2q of the LRP2 gene. This disorder is minimal in its studies as less than 30 cases have been recorded world wide. DBS/FOAR contains multiple characteristics in identifying the . The case belongs to the group of cervico-ocular-auditory dysplasias (Klippel-Feil syndrome). A strange feature in our case was the co-existence of conductive hypakousia in the right ear, due to congenital fixation of the stapes footplate, with perceptive deafness in the left ear, due to dysplasia of the cochlea and internal auditory by: