Literature DB >> 150559

Congenital X-linked adrenal hypoplasia.

P A Hensleigh, W V Moore, K Wilson, D Tulchinsky.   

Abstract

Fetal adrenal hypoplasia should be considered in pregnant patients with family histories of the condition and/or following observation of drastically reduced maternal estriol excretion. Antepartum diagnosis is important in the clinical management of these infants since deteriorating adrenal function frequently follows an asymptomatic period during the early neonatal life. Antepartum and neonatal diagnostic studies can identify fetal adrenal hypoplasia.

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Year:  1978        PMID: 150559

Source DB:  PubMed          Journal:  Obstet Gynecol        ISSN: 0029-7844            Impact factor:   7.661


  4 in total

Review 1.  Review: placental sulphatase deficiency.

Authors:  N F Taylor
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

2.  Familial X-linked adrenocortical hypoplasia association with androgenic precocity.

Authors:  D F Wittenberg
Journal:  Arch Dis Child       Date:  1981-08       Impact factor: 3.791

3.  Congenital adrenal hypoplasia, myopathy, and glycerol kinase deficiency: molecular genetic evidence for deletions.

Authors:  U Francke; J F Harper; B T Darras; J M Cowan; E R McCabe; A Kohlschütter; W K Seltzer; F Saito; J Goto; J P Harpey
Journal:  Am J Hum Genet       Date:  1987-03       Impact factor: 11.025

4.  Prenatal diagnosis of congenital lipoid adrenal hyperplasia (CLAH) by molecular genetic testing in Korean siblings.

Authors:  Hyun Sun Ko; Seungok Lee; Hyojin Chae; Sae Kyung Choi; Myungshin Kim; In Yang Park; Byung Kyu Suh; Jong Chul Shin
Journal:  Yonsei Med J       Date:  2011-11       Impact factor: 2.759

  4 in total

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