Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

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

JNMA; journal of the Nepal Medical Association - 1 Dec 2023

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

Abstract excerpt

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...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adrenal Hyperplasia, Congenital
Share to Androgens

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hypertension

Share to Hypothyroidism

Share to Mutation

Share to Steroid 11-beta-Hydroxylase

Source

Open in PubMed Open full text

Identifiers

PMID: 38289749
DOI: 10.31729/jnma.8378
PMCID: PMC10792719

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

11β Hydroxylase Deficiency in a Child with Hypothyroidism: A Case Report.PMID 38289749Read ↗

Congenital Adrenal Hyperplasia Case Attending With Hypertension Diagnosed With 21OH DeficiencySemantic proximity Read ↗

[Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency: late diagnosis and gender reassignment in a two-year-old child].Semantic proximity Read ↗

Congenital adrenal hyperplasia owing to 11β-hydroxylase deficiency.Semantic proximity Read ↗

Clinical perspectives in congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.Semantic proximity Read ↗

Partial deficiency of 17α-hydroxylase: a rare cause of congenital adrenal hyperplasia.Semantic proximity Read ↗

Steroid 11 beta-hydroxylase deficiency and related disorders.Semantic proximity Read ↗

[Clinical and genetic analysis of 11β-hydroxylase deficiency].Semantic proximity Read ↗

17α‑hydroxylase/17,20‑lyase deficiency in congenital adrenal hyperplasia: A case report.Semantic proximity Read ↗

Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiencySemantic proximity Read ↗

Multidisciplinary team management of 46,XY 17α-hydroxylase deficiency: a case report and literature review.Semantic proximity Read ↗

Novel homozygous p.Y395X mutation in the CYP11B1 gene found in a Vietnamese patient with 11β-hydroxylase deficiency.Semantic proximity Read ↗

High 17-hydroxyprogesterone level in newborn screening test for congenital adrenal hyperplasia.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.