Literature DB >> 3465177

Pathogenesis of congenital defects associated with Turner's syndrome: the role of hypoalbuminemia and edema.

T H Shepard, A G Fantel.   

Abstract

Studies of prenatal fetuses with 45,X Turner syndrome have allowed for plausible hypotheses of how their pitting edema may lead to production of the associated congenital defects found in the condition. Hypoalbuminemia in these fetuses which are only about one-sixth the levels found in newborns and one-third the level in "control" fetuses may explain the edema. Malformation of the ear, hairline, neck webbing, nipples, coarctation, nails and horseshoe kidney can be related to embryonic and fetal deformation from edema.

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Year:  1986        PMID: 3465177     DOI: 10.1530/acta.0.112s440

Source DB:  PubMed          Journal:  Acta Endocrinol Suppl (Copenh)        ISSN: 0300-9750


  3 in total

Review 1.  Chromosomal localisation of a gene(s) for Turner stigmata on Yp.

Authors:  T Ogata; C Tyler-Smith; S Purvis-Smith; G Turner
Journal:  J Med Genet       Date:  1993-11       Impact factor: 6.318

2.  Deletions spanning the neurofibromatosis 1 gene: identification and phenotype of five patients.

Authors:  L M Kayes; W Burke; V M Riccardi; R Bennett; P Ehrlich; A Rubenstein; K Stephens
Journal:  Am J Hum Genet       Date:  1994-03       Impact factor: 11.025

Review 3.  Turner syndrome and female sex chromosome aberrations: deduction of the principal factors involved in the development of clinical features.

Authors:  T Ogata; N Matsuo
Journal:  Hum Genet       Date:  1995-06       Impact factor: 4.132

  3 in total

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