Literature DB >> 1132883

Congenital sensori-neural deafness associated with onycho-osteo dystrophy and mental retardation (D.O.O.R. syndrome).

R J Cantwell.   

Abstract

A characteristic syndrome is described in which congenital sensori-neural deafness is associated not only with onychodystrophy but also with congenital bony anomalies the most characteristic of which are tri-phalangeal thumbs, bi-phalangeal digits of hands and feet, and dystrophic terminal phalanges of some of the fingers and toes. In addition, there is mental retardation and the dermatoglyphics are characterized by the presence of 10 arches and elevation of the atd angles. The syndrome is inherited as an autosomal recessive. It is suggested that this entity be named the D.O.O.R. Syndrome because of the deafness, onychodystrophy, osteodystrophy and retardation. A similar syndrome without retardation as described by Goodman et al. (1969) appears to be inherited as an autosomal dominant.

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Mesh:

Year:  1975        PMID: 1132883     DOI: 10.1007/bf00281463

Source DB:  PubMed          Journal:  Humangenetik        ISSN: 0018-7348


  3 in total

1.  Congenital deafness associated with onychodystrophy.

Authors:  M FEINMESSER; S ZELIG
Journal:  Arch Otolaryngol       Date:  1961-11

2.  [Familial deafness with osteo-onycho-dysplasia].

Authors:  R Walbaum; G Fontaine; J Lienhardt; J J Piquet
Journal:  J Genet Hum       Date:  1970-05

3.  Hereditary congenital deafness with onychodystrophy.

Authors:  R M Goodman; S Lockareff; G Gwinup
Journal:  Arch Otolaryngol       Date:  1969-10
  3 in total
  7 in total

1.  A new case of DOOR syndrome.

Authors:  Marzena Wiśniewska; Zofia Siwińska; Michał Felczak; Tomasz Wielkoszyński; Maciej Krawczyński; Anna Latos-Bieleńska
Journal:  J Appl Genet       Date:  2008       Impact factor: 3.240

2.  The deafness, onycho-osteo-dystrophy, mental retardation syndrome. Two new cases.

Authors:  O Sánchez; J J Mazas; I Ortíz; F de DeMatos
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Absence of Nails, Deaf-mutism, Seizures, and Intellectual Disability: A Case Report.

Authors:  Lal Devayanivasudevan Nair; Benjamin Sagayaraj; Radha Kumar
Journal:  J Clin Diagn Res       Date:  2015-04-01

Review 4.  Teratogenic inborn errors of metabolism.

Authors:  J V Leonard
Journal:  Postgrad Med J       Date:  1986-02       Impact factor: 2.401

5.  The genetic basis of DOORS syndrome: an exome-sequencing study.

Authors:  Philippe M Campeau; Dalia Kasperaviciute; James T Lu; Lindsay C Burrage; Choel Kim; Mutsuki Hori; Berkley R Powell; Fiona Stewart; Têmis Maria Félix; Jenneke van den Ende; Marzena Wisniewska; Hülya Kayserili; Patrick Rump; Sheela Nampoothiri; Salim Aftimos; Antje Mey; Lal D V Nair; Michael L Begleiter; Isabelle De Bie; Girish Meenakshi; Mitzi L Murray; Gabriela M Repetto; Mahin Golabi; Edward Blair; Alison Male; Fabienne Giuliano; Ariana Kariminejad; William G Newman; Sanjeev S Bhaskar; Jonathan E Dickerson; Bronwyn Kerr; Siddharth Banka; Jacques C Giltay; Dagmar Wieczorek; Anna Tostevin; Joanna Wiszniewska; Sau Wai Cheung; Raoul C Hennekam; Richard A Gibbs; Brendan H Lee; Sanjay M Sisodiya
Journal:  Lancet Neurol       Date:  2013-11-29       Impact factor: 44.182

6.  Anaesthetic management of an adult patient with DOOR syndrome: a case report.

Authors:  Pavel Michalek; William Donaldson; Alexander Abraham
Journal:  Cases J       Date:  2009-05-18

Review 7.  Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.

Authors:  Xue Gao; Pu Dai; Yong-Yi Yuan
Journal:  Hum Genet       Date:  2021-07-07       Impact factor: 4.132

  7 in total

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