Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
No clinical trials have been registered for familial isolated hypoparathyroidism due to impaired PTH secretion.
5 publications have been identified in PubMed for familial isolated hypoparathyroidism due to impaired PTH secretion. Research spans Case Report / Case Series (60%), Review / Meta-Analysis (20%), and Basic Science / Preclinical (20%).
Albert A (2025). [PMID: 40740723](https://pubmed.ncbi.nlm.nih.gov/40740723/). *Kidney Med*. [Review / Meta-Analysis]
Jiang Y (2025). [PMID: 40256360](https://pubmed.ncbi.nlm.nih.gov/40256360/). *Osteoporos Sarcopenia*. [Basic Science / Preclinical]
Mukhtar N (2024). [PMID: 39435356](https://pubmed.ncbi.nlm.nih.gov/39435356/). *Front Endocrinol (Lausanne)*. [Case Report / Case Series]
Thambundit A (2024). [PMID: 39439810](https://pubmed.ncbi.nlm.nih.gov/39439810/). *JCEM Case Rep*. [Case Report / Case Series]
Flottes Y (2024). [PMID: 38786528](https://pubmed.ncbi.nlm.nih.gov/38786528/). *Dent J (Basel)*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 5:40 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center