Neonatal diabetes mellitus with congenital hypothyroidism

MONDO:0012436

A rare genetic disease characterized by intrauterine growth retardation, permanent neonatal diabetes mellitus, and congenital hypothyroidism. Additional manifestations include congenital glaucoma, hepatic disease (hepatitis, fibrosis, and cirrhosis), polycystic kidneys, exocrine pancreatic dysfunction, sensorineural hearing impairment, developmental delay, and mild facial dysmorphism (such as flat nasal bridge, epicanthal folds, long philtrum, and low-set ears), among others

Also known as: NDH syndrome, neonatal diabetes mellitus with congenital hypothyroidism, NDH, Ndh syndrome, diabetes mellitus, neonatal, with congenital hypothyroidism, neonatal diabetes-congenital hypothyroidism-congenital glaucoma-hepatic fibrosis-polycystic kidneys syndrome

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

Follow this condition — get notified about new trials

Broader categories

Sort by