Literature DB >> 7774041

Familial microcephaly with severe neurological deficits: a description of five affected siblings.

V Gross-Tsur1, A Joseph, G Blinder, N Amir.   

Abstract

Autosomal recessive microcephaly is usually characterized by normal developmental milestones and minor neurological deficits. In this report, we describe five siblings in one family with marked microcephaly, intractable seizures, quadriplegia and profound mental retardation. The recurrence risk of microcephaly when associated with devastating neurological deficits, as exemplified by this family, may be high and in such cases, the role of appropriate genetic counseling is of utmost importance.

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Year:  1995        PMID: 7774041     DOI: 10.1111/j.1399-0004.1995.tb03918.x

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


  2 in total

1.  Loss of function of PCDH12 underlies recessive microcephaly mimicking intrauterine infection.

Authors:  Adi Aran; Nuphar Rosenfeld; Ranit Jaron; Paul Renbaum; Shachar Zuckerman; Hila Fridman; Sharon Zeligson; Reeval Segel; Yoav Kohn; Lara Kamal; Moien Kanaan; Yoram Segev; Eyal Mazaki; Ron Rabinowitz; Ori Shen; Ming Lee; Tom Walsh; Mary Claire King; Suleyman Gulsuner; Ephrat Levy-Lahad
Journal:  Neurology       Date:  2016-04-29       Impact factor: 9.910

2.  3-Phosphoglycerate dehydrogenase deficiency: an inborn error of serine biosynthesis.

Authors:  J Jaeken; M Detheux; L Van Maldergem; M Foulon; H Carchon; E Van Schaftingen
Journal:  Arch Dis Child       Date:  1996-06       Impact factor: 3.791

  2 in total

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