hrp0098p1-200 | Thyroid 2 | ESPE2024
Barskaya Maria
, Makretskaya Nina
, Demina Elena
, Petryaykina Elena
, Tiulpakov Anatoly
Background: Central congenital hypothyroidism (CCH) is a rare disorder. It may be a component of multiple pituitary hormone deficiency or (more rarely) represent an isolated entity, for which several monogenic causes are described.Aims: We report here a case of severe hypothyroidism caused by a novel homozygous variant in the TSHB gene.Results: The proband, a male from a c...