Literature DB >> 7337311

["De novo" partial trisomy 16p (author's transl)].

J Gabarrón Llamas, D Cabrerizo Portero, F Montserrat Bernal, T Rodríguez Costa, C Cabrerizo Merino, F Rodríguez López.   

Abstract

An additional small G-like chromosome was found in a six-months old male with multiple congenital anomalies and marked mental retardation. GTG banding revealed that the index patient was trisomic 16 q1100 leads to pter. In the bibliographical review a few cases of partial trisomy of chromosome 16 have been reported so far, but only two of them affect the same chromosomic region of our case, and only one of them is "de novo", like ours: this one would be the first case in the spanish bibliography, according to our knowledge. The clinical findings in our patient are similar to the other two cases published: our purpose is to contribute with a new case to delimitate what seems to be a definite phenotypical outline associated with trisomy 16p. The two patients early reported were females, the propositus is the first case of trisomy 16p reported in a male liveborn with genital anomalies.

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Mesh:

Year:  1981        PMID: 7337311

Source DB:  PubMed          Journal:  An Esp Pediatr        ISSN: 0302-4342


  2 in total

1.  Familial transmission of 16p trisomy in an infant.

Authors:  S M Jalal; D W Day; M Garcia; T Benjamin; J Rogers
Journal:  Hum Genet       Date:  1989-01       Impact factor: 4.132

2.  De novo duplication of chromosome 16p in a female infant with signs of neonatal hemochromatosis.

Authors:  Eva Maria Christina Schwaibold; Iris Bartels; Helmut Küster; Michael Lorenz; Peter Burfeind; Ronja Adam; Barbara Zoll
Journal:  Mol Cytogenet       Date:  2014-01-23       Impact factor: 2.009

  2 in total

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