Literature DB >> 6491641

[The 49,XYYYY syndrome: apropos of a case detected at birth and followed for 2 1/2 years].

H Plauchu, C Charrin, J C Kossmann.   

Abstract

A male child, mentally and physically retarded shows a facial dysmorphy, fingers' abnormalities and a radio-ulnar synostosis. These features are common in the 49,XYYYY syndrom, in which external genitalia, normal at birth, remain undevelopped at the time of puberty. Four others publications through the literature report tetrasomic cells for Y chromosome, but only two of them are real 49,XYYYY (with 88% to 100% of affected cells). Our case has 96,7% tetrasomic cells.

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Mesh:

Year:  1984        PMID: 6491641

Source DB:  PubMed          Journal:  J Genet Hum        ISSN: 0021-7743


  2 in total

1.  Structure and function of ribosomal protein S4 genes on the human and mouse sex chromosomes.

Authors:  A R Zinn; R K Alagappan; L G Brown; I Wool; D C Page
Journal:  Mol Cell Biol       Date:  1994-04       Impact factor: 4.272

Review 2.  Autism spectrum disorder associated with 49,XYYYY: case report and review of the literature.

Authors:  Caroline Demily; Alice Poisson; Elodie Peyroux; Valérie Gatellier; Alain Nicolas; Caroline Rigard; Caroline Schluth-Bolard; Damien Sanlaville; Massimiliano Rossi
Journal:  BMC Med Genet       Date:  2017-01-31       Impact factor: 2.103

  2 in total

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