Laurence-Moon syndrome

MONDO:0009514

A very rare genetic multisystemic disorder characterized by pituitary dysfunction, ataxia, peripheral neuropathy, spastic paraplegia, and chorioretinal dystrophy.

Also known as: LMS, Laurence-Moon syndrome, LNMS, Laurence-MOON syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Laurence-Moon syndrome itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Syndromic disease (7158) ↑ Autosomal recessive disease (999) ↑ Congenital hypogonadotropic hypogonadism (83) ↑ Multiple congenital anomalies/dysmorphic syndrome-intellectual disability (59)

Including sub-types (0) Tagged with Laurence-Moon syndrome (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.