Literature DB >> 7193414

Holoprosencephaly and endocrine dysgenesis in brothers.

M L Begleiter, D J Harris.   

Abstract

We report 2 brothers with holoprosencephaly, endocrine dysgenesis, and micropenis. This combination has been reported once previously in sibs (2 sisters) by Hintz et al (1968). In that case, autosomal recessive inheritance may have been the cause. The same may be true in our patients, but X-linked recessive inheritance is not excluded.

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Year:  1980        PMID: 7193414     DOI: 10.1002/ajmg.1320070312

Source DB:  PubMed          Journal:  Am J Med Genet        ISSN: 0148-7299


  4 in total

1.  Molecular detection of a Yp/18 translocation in a 45,X holoprosencephalic male.

Authors:  M Münke; D C Page; L G Brown; B A Armson; E H Zackai; M T Mennuti; B S Emanuel
Journal:  Hum Genet       Date:  1988-11       Impact factor: 4.132

2.  What is the incidence of holoprosencephaly?

Authors:  E S Saunders; D Shortland; P M Dunn
Journal:  J Med Genet       Date:  1984-02       Impact factor: 6.318

3.  Holoprosencephaly: a family showing dominant inheritance and variable expression.

Authors:  A L Collins; P W Lunt; C Garrett; N R Dennis
Journal:  J Med Genet       Date:  1993-01       Impact factor: 6.318

Review 4.  Stem cell function and plasticity in the normal physiology of the adrenal cortex.

Authors:  Gary D Hammer; Kaitlin J Basham
Journal:  Mol Cell Endocrinol       Date:  2020-10-12       Impact factor: 4.102

  4 in total

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