11β Hydroxylase Deficiency in a Child with Hypothyroidism: A Case Report

Bipesh Kumar Shah, Richa Koirala, Sumit Dhamala, Mukesh Bhatta, Shekhar Khatiwada · 2023

Read 11β Hydroxylase Deficiency in a Child with Hypothyroidism: A Case Report by Bipesh Kumar Shah, Richa Koirala, Sumit Dhamala, Mukesh Bhatta, Shekhar Khatiwada (2023) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-10792719.txt.

Description

Bipesh Kumar Shah and co-authors reported this 2023 case of a child with two hormone disorders at once. Congenital adrenal hyperplasia stems from enzyme faults in the adrenal glands. One form, from a missing hydroxylase enzyme, is the second most common type. It drives blood pressure up and pushes male hormone effects too far, sometimes harming organs in children.

Their patient was a ten-year-old boy already on thyroid replacement for an underactive thyroid. He arrived with severe high blood pressure and signs of androgen excess. Testing traced both problems to the adrenal enzyme fault. The case reminds clinicians that dangerous pressure in a child can hide a gland disorder, and that two hormone conditions can coexist in one patient.

Catalog record

CREATORBipesh Kumar Shah, Richa Koirala, Sumit Dhamala, Mukesh Bhatta, Shekhar Khatiwada
YEAR2023
COLLECTIONPAPERS
FORMATTXT
FILE SIZE7 KB
VERSION1.0
LICENSECC BY 4.0
RIGHTSCC BY
SOURCEEurope PMC

Source: https://europepmc.org/articles/PMC10792719

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