Literature DB >> 8256819

DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.

H J Lin1, E D Kakkis, D J Eteson, R S Lachman.   

Abstract

We report the seventeenth case of the recessive form of the DOOR syndrome. The parents were Guatemalan and not known to be consanguineous. The patient had developmental delay, severe sensorineural deafness, and abnormal nails and phalanges in the hands and feet. Urinary 2-oxoglutarate excretion was normal. The patient was among a subset of DOOR syndrome patients without seizures in infancy. This observation may be useful in discussing the prognosis for newly identified cases.

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Year:  1993        PMID: 8256819     DOI: 10.1002/ajmg.1320470419

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  2 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.  Dominant deafness-onychodystrophy syndrome caused by an ATP6V1B2 mutation.

Authors:  Ibis Menendez; Claudia Carranza; Mariana Herrera; Nely Marroquin; Joseph Foster; Filiz Basak Cengiz; Guney Bademci; Mustafa Tekin
Journal:  Clin Case Rep       Date:  2017-02-08
  2 in total

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