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Bookmark or Share- Entry - #245800 - LAURENCE-MOON SYNDROME; LNMS - OMIMLaurence-Moon syndrome (LNMS) has a clinical presentation similar to that of Oliver-McFarlane syndrome (275400), including chorioretinopathy and pituitary dysfunction, but with childhood onset of ataxia, peripheral neuropathy, and spastic paraplegia and without trichomegaly.
- Orphanet: Laurence-Moon syndromeLikely pathogenic or pathogenic variants in the PNPLA6 gene have been identified in patients with Laurence-Moon syndrome (LMS).
- Laurence-moon syndrome | About the Disease | GARD - Genetic and Rare ...When Do Symptoms of Laurence-moon syndrome Begin? Symptoms of this disease may start to appear as a Newborn. The age symptoms may begin to appear differs between diseases.
- Laurence-Moon syndrome - Health JadeLaurence-Moon syndrome (LNMS or LMS), also called Laurence-Moon-Biedl syndrome (LMBBS) because of similarities with Bardet-Biedl syndrome (BBS), is a very rare genetic disorder that affects many parts of the body characterized by underactive pituitary gland (occurs when the pituitary gland doesn’t produce the right amount of hormones), ataxia ...
- Laurence-Moon-Bardet-Biedl Syndrome Diagnosis - Verywell HealthIn previous years, Laurence-Moon-Bardet-Biedl syndrome (LMBBS) was a term used to describe an inherited genetic condition that affected approximately 1 in 100,000 babies born. It was named after the four doctors who initially described the symptoms of the syndrome.
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