Literature DB >> 16429203

[Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency].

Ramires Tosatti Júnior1, Haroldo Silva de Souza, Alexandre Tosatti.   

Abstract

The objective of this article is to relate the diagnostic and clinical evolution of a 15 year old patient with a congenital adrenal steroidogenesis dysfunction that can present as hypertension diagnosed later in life (adolescence), virilization or salt wasting (birth and childhood).

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Year:  2006        PMID： 16429203     DOI： 10.1590/s0066-782x2005001900008

Source DB:  PubMed          Journal:  Arq Bras Cardiol        ISSN： 0066-782X            Impact factor:   2.000


  4 in total

Review 1.  [Change in stature after pseudo-puberty early by 11ß hydroxylase deficiency in a girl of 7 years: report of a case and review of literature].

Authors:  Hanane Latrech; Ahmed Gaouzi
Journal:  Pan Afr Med J       Date:  2015-02-23

2.  A child with hypertension and ambiguous genitalia - an uncommon variant of congenital adrenal hyperplasia: a case report.

Authors:  Vivek Pant; Suman Baral; Bishal Shrestha; Arjun Tumbapo
Journal:  J Med Case Rep       Date:  2017-06-23

3.  Male Gender Identity and Reversible Hypokalemic Hypertension in a 46,XX Child with 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia.

Authors:  Alpesh Goyal; Hiya Boro; Rajesh Khadgawat
Journal:  Cureus       Date:  2019-07-26

4.  An Association of Chronic Hyperaldosteronism with Medullary Nephrocalcinosis.

Authors:  Kartik Mittal; Karan Anandpara; Amit K Dey; Rajaram Sharma; Hemangini Thakkar; Priya Hira; Hemant Deshmukh
Journal:  Pol J Radiol       Date:  2015-09-05
  4 in total

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