Literature DB >> 7416109

Partial trisomy 9q due to maternal 9/17 translocation.

S F Aftimos, J J Hoo, M I Parslow.   

Abstract

A patient with partial trisomy 9q due to material 9/17 translocation was studied and compared with four previously reported cases. The similarity of their clinical features allowed us to delineate a distinct clinical syndrome, which is characterized by psychomotor retardation, dolichocephaly, beaked nose, deep-seated eyes, and long fingers and toes. There is an overlap between some of the features of this syndrome and those of trisomy 9.

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Year:  1980        PMID: 7416109     DOI: 10.1001/archpedi.1980.02130210032009

Source DB:  PubMed          Journal:  Am J Dis Child        ISSN: 0002-922X


  3 in total

1.  Identification of an unbalanced cryptic translocation t(9;17)(q34.3;p13.3) in a child with dysmorphic features.

Authors:  A M Estop; P A Mowery-Rushton; K M Cieply; S J Kochmar; C R Sherer; M Clemens; U Surti; E McPherson
Journal:  J Med Genet       Date:  1995-10       Impact factor: 6.318

2.  Duplication 9q34 syndrome.

Authors:  P W Allderdice; B Eales; H Onyett; W Sprague; K Henderson; P A Lefeuvre; G Pal
Journal:  Am J Hum Genet       Date:  1983-09       Impact factor: 11.025

3.  Double partial trisomy 9q34.1-->qter and 21pter-->q22.11: FISH and clinical findings.

Authors:  T Mattina; M Pierluigi; D Mazzone; S Scardilli; C Perfumo; F Mollica
Journal:  J Med Genet       Date:  1997-11       Impact factor: 6.318

  3 in total

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