A newborn with ambiguous genitalia and persistent hypoglycemia

A newborn with ambiguous genitalia and persistent hypoglycemia

Educational Objectives: In patients with classical 21-hydroxylase deficiency, the metabolic block in aldosterone and cortisol synthe-sis results in raised hormone precursor, 17-hydroxyprogesterone. Infants with simple virilizing congenital adrenal hyperplasia do not produce cortisol efficiently; how...

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Main Authors: Salleh, Muhammad Farhan, Lai, Yin Ye, Mohamed Mokhtar, Normaizuwana, Thambiah, Subashini C., Samsudin, Intan Nureslyna
Format: Article
Published: SAGE Publications Inc. 2024
Online Access:http://psasir.upm.edu.my/id/eprint/113890/
https://journals.sagepub.com/doi/10.1177/00099228241271944
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Institution: Universiti Putra Malaysia
id my.upm.eprints.113890
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spelling my.upm.eprints.1138902025-02-05T03:27:19Z http://psasir.upm.edu.my/id/eprint/113890/ A newborn with ambiguous genitalia and persistent hypoglycemia Salleh, Muhammad Farhan Lai, Yin Ye Mohamed Mokhtar, Normaizuwana Thambiah, Subashini C. Samsudin, Intan Nureslyna Educational Objectives: In patients with classical 21-hydroxylase deficiency, the metabolic block in aldosterone and cortisol synthe-sis results in raised hormone precursor, 17-hydroxyprogesterone. Infants with simple virilizing congenital adrenal hyperplasia do not produce cortisol efficiently; however, they can synthesize adequate aldosterone to maintain salt-water balance. SAGE Publications Inc. 2024-08 Article PeerReviewed Salleh, Muhammad Farhan and Lai, Yin Ye and Mohamed Mokhtar, Normaizuwana and Thambiah, Subashini C. and Samsudin, Intan Nureslyna (2024) A newborn with ambiguous genitalia and persistent hypoglycemia. Clinical Pediatrics. ISSN 0009-9228; eISSN: 1938-2707 https://journals.sagepub.com/doi/10.1177/00099228241271944 10.1177/00099228241271944
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
description Educational Objectives: In patients with classical 21-hydroxylase deficiency, the metabolic block in aldosterone and cortisol synthe-sis results in raised hormone precursor, 17-hydroxyprogesterone. Infants with simple virilizing congenital adrenal hyperplasia do not produce cortisol efficiently; however, they can synthesize adequate aldosterone to maintain salt-water balance.
format Article
author Salleh, Muhammad Farhan
Lai, Yin Ye
Mohamed Mokhtar, Normaizuwana
Thambiah, Subashini C.
Samsudin, Intan Nureslyna
spellingShingle Salleh, Muhammad Farhan
Lai, Yin Ye
Mohamed Mokhtar, Normaizuwana
Thambiah, Subashini C.
Samsudin, Intan Nureslyna
A newborn with ambiguous genitalia and persistent hypoglycemia
author_facet Salleh, Muhammad Farhan
Lai, Yin Ye
Mohamed Mokhtar, Normaizuwana
Thambiah, Subashini C.
Samsudin, Intan Nureslyna
author_sort Salleh, Muhammad Farhan
title A newborn with ambiguous genitalia and persistent hypoglycemia
title_short A newborn with ambiguous genitalia and persistent hypoglycemia
title_full A newborn with ambiguous genitalia and persistent hypoglycemia
title_fullStr A newborn with ambiguous genitalia and persistent hypoglycemia
title_full_unstemmed A newborn with ambiguous genitalia and persistent hypoglycemia
title_sort newborn with ambiguous genitalia and persistent hypoglycemia
publisher SAGE Publications Inc.
publishDate 2024
url http://psasir.upm.edu.my/id/eprint/113890/
https://journals.sagepub.com/doi/10.1177/00099228241271944
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