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

[Male pseudohermaphroditism due to 17-alpha-hydroxylase deficiency].

Minerva endocrinologica - 1 Dec 1995

Bartolucci L, Fioretti M, Rossi G, Commissari R, Valori C

Abstract excerpt

A case of 17-alpha-hydroxylase deficiency in a genotypic male is described. The patient, who had grown up as a female, at the age of 18 years by chance was seen for enteritis. She presented primary amenorrhea and lack of secondary sexual characteristics combined with hypertension and mild hypokalemia due to excess of mineralcorticoids. The hormonal profile observed under basal conditions was evocative of a...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to Adrenal Hyperplasia, Congenital
Share to Aldosterone

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Diagnosis, Differential

Share to Disorders of Sex Development

Share to Genotype

Source

Identifiers

PMID: 8709921

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Male pseudohermaphroditism due to 17-alpha-hydroxylase deficiency].PMID 8709921Read ↗

[Male pseudohermaphroditism due to 17 beta-hydroxysteroid dehydrogenase deficiency].Semantic proximity Read ↗

Female phenotype with male karyotype: a clinical enigma.Semantic proximity Read ↗

A Rare Case of 45,X[5]/46XX[55] 21-Hydroxylase Deficiency with Female Pseudohermaphroditism and a Giant Uterine Fibroid: Diagnosis and TreatmentSemantic proximity Read ↗

[Male pseudohermaphroditism].Semantic proximity Read ↗

Male pseudohermaphroditism.Semantic proximity Read ↗

[Inappropriate sexual differentiation of sex reversal type in 16-year-old boy with male phenotype].Semantic proximity Read ↗

[Disorder of androgen biosynthesis].Semantic proximity Read ↗

[Male pseudohermaphroditism. State and present problems (author's transl)].Semantic proximity Read ↗

[Male pseudohermaphroditism due to disorder of androgen receptor function].Semantic proximity Read ↗

Female pseudohermaphroditism and inefficient peak bone mass in an untreated subject affected by 21-hydroxylase congenital adrenal hyperplasia.Semantic proximity Read ↗

17beta-hydroxysteroid dehydrogenase 3 deficiency in a male pseudohermaphrodite.Semantic proximity Read ↗

Male pseudohermaphroditism due to 5 alpha-reductase-2 deficiency in an Arab kindred.Semantic proximity Read ↗

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