Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.

doi:10.1210/jcem.83.5.4815

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Article

Familial dysalbuminemic hypertriiodothyroninemia: a new, dominantly inherited albumin defect.

The Journal of clinical endocrinology and metabolism - 1 May 1998

Sunthornthepvarakul T, Likitmaskul S, Ngowngarmratana S, Angsusingha K, Kitvitayasak S, Scherberg N H, Refetoff S

Abstract excerpt

We report the abnormal albumin in members of a Thai family that presented with high serum total T3 but not T4 when measured by radioimmunoassay. In contrast, total T3 values were very low when measured by ELISA and chemiluminescence. The subjects have no goiter, and clinically euthyroid. Their se...

Topics

Alleles
DNA Mutational Analysis
Female
Genotype
Humans
Hyperthyroidism
Immunosorbent Techniques
Infant, Newborn
Mutation
Pedigree
Serum Albumin
Thailand
Thyroxine
Triiodothyronine

Source

Open in PubMed

Identifiers

PMID: 9589637
DOI: 10.1210/jcem.83.5.4815

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-9589637-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 Aug 2026.

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