Literature DB >> 24605732

Congenital adrenal hyperplasia with cholestatic jaundice.

Nisreen Feroz Ali1, Farhana Zafar2, Areeb Sohail Bangash2, Abdul Malik2, Karimunnisa Mohammedi2.   

Abstract

Congenital Adrenal Hyperplasia describes a group of autosomal recessive disorders characterized by a decrease in Cortisol production. 11 beta hydroxylase deficiencies is the second most common form. However, its presentation with cholestatic jaundice is extremely rare. We present a case of a 29-day-old infant who came to us with unusual dark complexion, persistent jaundice, and electrolyte imbalance. On investigation he was diagnosed as a case of congenital adrenal hyperplasia. Treatment with hydrocortisone and fludrocortisone cleared his jaundice and complexion with subsequent improvement in electrolytes. The aim of this report is to illustrate an unusual presentation of CAH with Cholestatic jaundice. This is the first case to be reported from Pakistan. The case outlines the difficult workup that was encountered in the diagnosis and management of the patient.

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Year:  2014        PMID: 24605732

Source DB:  PubMed          Journal:  J Pak Med Assoc        ISSN: 0030-9982            Impact factor:   0.781


  1 in total

1.  A neonate with poor weight gain and hyperkalemia: Answers.

Authors:  Chiung-Chen Liu; Shih-Hua Lin; Chih-Chien Sung; Chien-Ming Lin
Journal:  Pediatr Nephrol       Date:  2015-12-01       Impact factor: 3.714

  1 in total

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