Publication: 11β Hydroxylase Deficiency in a Child with Hypothyroidism: A Case Report
| creativeworkseries.issn | JNMA Print ISSN: 0028-2715; Online ISSN: 1815-672X | |
| dc.contributor.author | Shah, Bipesh Kumar | |
| dc.contributor.author | Koirala, Richa | |
| dc.contributor.author | Dhamala, Sumit | |
| dc.contributor.author | Bhatta, Mukesh | |
| dc.contributor.author | Khatiwada, Shekhar | |
| dc.date.accessioned | 2025-08-21T05:11:26Z | |
| dc.date.available | 2025-08-21T05:11:26Z | |
| dc.date.issued | 2023 | |
| dc.description | Authors Bipesh Kumar Shah Department of Paediatrics, B.P. Koirala Institute of Health Sciences, Dharan, Sunsari, Nepal Richa Koirala B.P. Koirala Institute of Health Sciences, Dharan, Sunsari, Nepal Sumit Dhamala B.P. Koirala Institute of Health Sciences, Dharan, Sunsari, Nepal Mukesh Bhatta Department of Paediatrics, B.P. Koirala Institute of Health Sciences, Dharan, Sunsari, Nepal Shekhar Khatiwada B.P. Koirala Institute of Health Sciences, Dharan, Sunsari, Nepal | |
| dc.description.abstract | Abstract Congenital adrenal hyperplasia occurs due to enzymatic defects in the adrenocortical steroidogenesis. 11β hydroxylase deficiency is the second most common cause of congenital adrenal hyperplasia which presents with hypertension and features of androgen excess. Hypertension has also been found to cause end-organ damage in children with 11β hydroxylase deficiency. We report a case of a 10-year-old male child with hypothyroidism under thyroid replacement therapy, presenting with features of severe hypertension and androgen excess, later on, diagnosed as congenital adrenal hyperplasia due to 11β hydroxylase deficiency. | |
| dc.identifier | https://doi.org/10.31729/jnma.8378 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.14572/1840 | |
| dc.language.iso | en_US | |
| dc.publisher | Nepal Medical Association | |
| dc.title | 11β Hydroxylase Deficiency in a Child with Hypothyroidism: A Case Report | |
| dc.type | Other | |
| dspace.entity.type | Publication | |
| local.article.type | Case Report | |
| oaire.citation.endPage | 957 | |
| oaire.citation.startPage | 956 | |
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