Literature DB >> 3608216

Syndrome of microcephaly, deafness/malformed ears, mental retardation and peculiar facies in a mother and son.

H Kawashima, N Tsuji.   

Abstract

We report a mother and son who have a microcephaly with a characteristic dysmorphic face. Prominent manifestations include facial asymmetry, prominent glabella, deafness, low-set, cup-shaped ears, thick, protruding lower lip, micrognathia, and mental retardation. We conclude that these patients have a previously undescribed type of genetic microcephaly. The mother has become normocephalic and we would not have been able to diagnose her condition without her childhood photographs. Such photographs are essential in the recognition of familial syndromes.

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Year:  1987        PMID: 3608216     DOI: 10.1111/j.1399-0004.1987.tb02812.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN: 0009-9163            Impact factor:   4.438


  2 in total

1.  Electrophysiological detection of scalar changing perimodiolar cochlear electrode arrays: a long term follow-up study.

Authors:  Philipp Mittmann; I Todt; A Ernst; G Rademacher; S Mutze; S Göricke; M Schlamann; R Ramalingam; S Lang; F Christov; D Arweiler-Harbeck
Journal:  Eur Arch Otorhinolaryngol       Date:  2016-06-28       Impact factor: 2.503

2.  A dominantly inherited syndrome (microcephaly, short stature, peculiar facies, mental retardation) associated with two balanced rearrangements involving chromosomes 2;7 and 5;20.

Authors:  R Vivarelli; O Zuffardi; P Maraschio; C Anichini; R Scarinci
Journal:  Hum Genet       Date:  1988-08       Impact factor: 4.132

  2 in total

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