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Article

Familial Dysalbuminemic Hyperthyroxinemia (FDH), Albumin Gene Variant (R218S), and Risk of Miscarriages in Offspring.

The American journal of the medical sciences - 1 Nov 2020

Lai Shuiqing, Gopalakrishnan Geetha, Li Jie, Liu Xin, Chen Yuancheng, Wen Yuqiong, Zhang Shuting, Huang Bizhu, Phornphutkul Chanika, Liu Simin, Kuang Jian

Abstract excerpt

BACKGROUND: Familial dysalbuminemic hyperthyroxinemia (FDH) is a rare autosomal dominant disorder whose clinical characteristics remain incompletely understood, we investigated the role of albumin gene mutation in relation to miscarriage rate in a large pedigree of FDH followed up for 4 years. PATIENTS AND METHODS: The proband and extended family with unexplained miscarriage and hyperthyroxinemia were identified...

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Identifiers

PMID: 32665066
DOI: 10.1016/j.amjms.2020.05.035

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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