Literature DB >> 9350825

Isolated sacral agenesis in a fetus monosomic for 7q36.1-->qter.

N M Savage1, N A Maclachlan, C A Joyce, I E Moore, J A Crolla.   

Abstract

A fetus with severe sacral agenesis and intrauterine growth retardation, ascertained at prenatal diagnosis, was found to be carrying an unbalanced form of a paternal balanced reciprocal translocation (7;19)(q36.1;q13.43), resulting in functional monosomy for 7q36.1-->qter. Necropsy confirmed that the fetus had isolated sacral agenesis type II. A critical region for autosomal dominant sacral agenesis has recently been mapped to the 7q36 region. This case provides further evidence for a sacral agenesis locus in this region and may help to refine the critical region further.

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Year:  1997        PMID: 9350825      PMCID: PMC1051099          DOI: 10.1136/jmg.34.10.866

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


  13 in total

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7.  Physical mapping of the holoprosencephaly critical region on chromosome 7q36.

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Journal:  Nat Genet       Date:  1993-03       Impact factor: 38.330

Review 8.  Holoprosencephaly and sacral agenesis in a fetus with a terminal deletion 7q36-->7qter.

Authors:  N Morichon-Delvallez; A L Delezoide; M Vekemans
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Review 9.  Case reports of malformations associated with maternal diabetes: history and critique.

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10.  A five-generation family with sacral agenesis and spina bifida: possible similarities with the mouse T-locus.

Authors:  M Fellous; J Boué; C Malbrunot; E Wollman; M Sasportes; N Van Cong; A Marcelli; R Rebourcet; C Hubert; F Demenais; R C Elston; K K Namboodiri; E B Kaplan; M Fellous
Journal:  Am J Med Genet       Date:  1982-08
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3.  7q36 deletion and 9p22 duplication: effects of a double imbalance.

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  3 in total

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