Literature DB >> 1086627

[Holoprosencephaly by triploidy 69 XXX in a 5 month old fetus].

J M Emberger, C Marty-Double, D Pincemin, J Caderas de Kerleau.   

Abstract

Microcephaly, occipital meningocele, and uveal coloboma were observed in a 5-month-old fetus with a 69, XXX karyotype. Autopsy showed an holoprosencephaly, which has never before been reported in triploidy.

Entities:  

Mesh：

Year:  1976        PMID： 1086627

Source DB:  PubMed          Journal:  Ann Genet        ISSN： 0003-3995


  4 in total

1.  A case of suspected teratogenic holoprosencephaly.

Authors:  M Stabile; A Bianco; S Iannuzzi; M C Buonocore; V Ventruto
Journal:  J Med Genet       Date:  1985-04       Impact factor: 6.318

2.  Descriptive neuropathology of chromosomal disorders in man.

Authors:  F Gullotta; H Rehder; A Gropp
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Triploidy with cyclopia and identical HLA alleles in the parents.

Authors:  J C Lambert; P Philip; G Charpentier; M Ferrari; M Donzeau; N Ayraud
Journal:  J Med Genet       Date:  1984-02       Impact factor: 6.318

4.  Semilobar holoprosencephaly in a 12-month-old baby boy born to a primigravida patient with type 1 diabetes mellitus: a case report.

Authors:  Pedro Pallangyo; Frederick Lyimo; Paulina Nicholaus; Hilda Makungu; Maria Mtolera; Isaac Mawenya
Journal:  J Med Case Rep       Date:  2016-12-20
  4 in total

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