Literature DB >> 22815032

Congenital adrenal hyperplasia masquerading as periodic paralysis in an adolescent girl.

Anjali Sathya1, R Ganesan, Arun Kumar.   

Abstract

Congenital adrenal hyperplasia is an uncommon diagnosis in routine clinical practice. 21-hydroxylase deficiency, which is its most common subtype, may be diagnosed at birth in a female infant by virilisation or by features of salt wasting in both genders. However, other uncommon subtypes of this condition such as 17-alpha-hydroxylase deficiency, 11-beta-hydroxylase deficiency may present much later in adolescence or adulthood. A high index of suspicion is necessary when evaluating children with hypertension, hypokalaemia, metabolic alkalosis or sexual infantilism.

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Year:  2012        PMID: 22815032

Source DB:  PubMed          Journal:  Singapore Med J        ISSN: 0037-5675            Impact factor:   1.858


  3 in total

Review 1.  Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Authors:  Krupali Bulsari; Henrik Falhammar
Journal:  Endocrine       Date:  2016-12-07       Impact factor: 3.633

2.  A challenging case of primary amenorrhoea.

Authors:  Vijaya Sarathi; Ramesh Reddy; Sridevi Atluri; Channabasappa Shivaprasad
Journal:  BMJ Case Rep       Date:  2018-07-11

3.  Congenital Adrenal Hyperplasia and Schmid Metaphyseal Chondrodysplasia in a Child.

Authors:  Efat Khorasani; Rahim Vakili
Journal:  Iran J Med Sci       Date:  2016-01
  3 in total

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