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Classic galactosemia

MONDO:0009258

Classic galactosemia is a life-threatening metabolic disease with onset in the neonatal period. Infants usually develop feeding difficulties, lethargy, and severe liver disease.

Also known as: GALT deficiency, classic galactosemia, galactose-1-phosphate uridyltransferase deficiency, galactosemia type 1, classical galactosemia, homozygous duarte-type, Galt deficiency, galactose-1-phosphate uridylyltransferase deficiency, galactosemia

7 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Infertility disorder (336) Metabolic disease (233) Hereditary disease (176) Eye disorder (102) Female infertility (100) Endocrine system disorder (72) Primary ovarian failure (48) Inborn errors of metabolism (45) Female reproductive system disorder (27)

Trials to join now! 2 Not yet recruiting 1 Completed 4

IVF Needle-Free? oral pill tested as injection alternative

Disease control Not yet recruiting

This trial tests whether an oral medication called linzagolix can replace daily injections used to prevent premature ovulation during in vitro fertilization (IVF). The study compares the number of mature eggs retrieved in women taking the pill versus those receiving standard inje…

Sponsor: Centro A.M.B.R.A. (Associazione Medici e Biologi per la Riproduzione Assistita) • Aim: Disease control

Last updated Aug 05, 2026 00:00 UTC