Laurence–Moon syndrome (LMS) is a rare autosomal recessive  genetic disorder associated with retinitis pigmentosa, extra digits, spastic paraplegia, hypogonadism ...
Laurence-Moon syndrome ; Disorder Subdivisions. ... Bardet-Biedl syndrome shows significant overlap with a disorder called Laurence-Moon syndrome.
Laurence-Moon Syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Bardet-Biedl syndrome is a disorder that affects many parts of the body. The signs and symptoms of this condition vary among affected individuals, even ...
Laurence-Moon-Bardet-Biedl syndrome (LMBBS) is an inherited genetic condition that affects approximately 1 in 100,000 babies born. It is named after the ...
Clinical Synopsis : TEXT: A number sign (#) is used with this entry because of evidence that Laurence-Moon syndrome (LNMS) is caused by compound heterozygous mutation ...
Lau·rence-Moon syn·drome (law'rĕnts mūn), [MIM*245800] disorder characterized by mental retardation, pigmentary retinopathy, hypogenitalism, and spastic ...
Synonyms: adipogenital-retinitis pigmentosa syndrome, LM syndrome This is a rare autosomal recessive condition. Laurence-Moon-Biedl syndrome and Laurence-Moon-Biedl ...
The Laurence-Moon-Bardet-Biedl Society is the only registered charity supporting people with Laurence-Moon-Bardet-Biedl Syndrome, ... LMBBS or have the syndrome ...
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