Literature DB >> 8882787

Further delineation of the acro-renal-ocular syndrome.

C M Aalfs1, M J van Schooneveld, E M van Keulen, R C Hennekam.   

Abstract

A triad of acral, renal, and ocular abnormalities was reported previously in four families. We report on a fifth family, in which a mother, one of her four sons and one of her two daughters are affected. Major findings in the acro-renal-ocular syndrome are upper limb abnormalities, mainly thumb hypoplasia, eye abnormalities such as coloboma and Duane anomaly and renal migration defects. A close embryological-temporal relationship between the traits of this entity suggest a common monogenic cause. The pattern of inheritance is probably autosomal dominant. Because of a wide variability of clinical manifestations, recognition of the syndrome in individual cases may be difficult.

Entities:  

Mesh:

Year:  1996        PMID: 8882787     DOI: 10.1002/(SICI)1096-8628(19960329)62:3<276::AID-AJMG14>3.0.CO;2-H

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


  4 in total

Review 1.  Ocular coloboma: a reassessment in the age of molecular neuroscience.

Authors:  C Y Gregory-Evans; M J Williams; S Halford; K Gregory-Evans
Journal:  J Med Genet       Date:  2004-12       Impact factor: 6.318

2.  Dandy-Walker malformation, genitourinary abnormalities, and intellectual disability in two families.

Authors:  Maha S Zaki; Amira Masri; Anne Gregor; Joseph G Gleeson; Rasim Ozgur Rosti
Journal:  Am J Med Genet A       Date:  2015-06-24       Impact factor: 2.802

3.  Congenital third cranial nerve palsy with prenuclear dysinnervation involving otolithic pathways: Underpinnings of a novel congenital cranial dysinnervation disorder.

Authors:  Pramod K Pandey; Divya Kishore; Annu Joon; Priya Saraf
Journal:  Indian J Ophthalmol       Date:  2020-07       Impact factor: 1.848

4.  Two missense mutations in SALL4 in a patient with microphthalmia, coloboma, and optic nerve hypoplasia.

Authors:  E Ullah; D Wu; L Madireddy; R Lao; P Ling-Fung Tang; E Wan; T Bardakjian; S Kopinsky; P-Y Kwok; A Schneider; S Baranzini; M Ansar; A Slavotinek
Journal:  Ophthalmic Genet       Date:  2016-09-23       Impact factor: 1.803

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.