Literature DB >> 4039890

X-linked syndrome of branchial arch and other defects.

H V Toriello, J V Higgins, J Abrahamson, D F Waterman, W D Moore.   

Abstract

We report on two brothers and their maternal first cousin who have branchial arch defects and other anomalies. Similar physical findings in all three include microcephaly, downslanting palpebral fissures, highly arched palate, apparently lowset, protruding ears, bilateral hearing loss, slightly webbed neck, and mild short stature. In addition, two boys had cryptorchidism, and one had subvalvar pulmonic stenosis and body asymmetry. We suggest that these cousins have an X-linked syndrome of which branchial arch defects are a component. Other pleiotropic manifestations of the mutant gene include microcephaly and cryptorchidism; body asymmetry and relatively short stature may be components as well.

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Year:  1985        PMID: 4039890     DOI: 10.1002/ajmg.1320210120

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


  3 in total

Review 1.  X linked mental retardation.

Authors:  I A Glass
Journal:  J Med Genet       Date:  1991-06       Impact factor: 6.318

2.  Clinical and molecular studies in four patients with SRY-positive 46,XX testicular disorders of sex development: implications for variable sex development and genomic rearrangements.

Authors:  Shinichi Nakashima; Akira Ohishi; Fumio Takada; Hideki Kawamura; Maki Igarashi; Maki Fukami; Tsutomu Ogata
Journal:  J Hum Genet       Date:  2014-08-07       Impact factor: 3.172

Review 3.  Review of the Genetic Basis of Jaw Malformations.

Authors:  Mairaj K Ahmed; Xiaoqian Ye; Peter J Taub
Journal:  J Pediatr Genet       Date:  2016-10-12
  3 in total

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