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Laurence-Moon Syndrome

Disease Launois-Bensaude syndromeLaurence-moon-biedl syndrome

Laurence-Moon syndrome is characterized by obesity, intellectual disability, retinitis pigmentosa, and polydactyly.

 


Laurence-Moon Syndrome is a rare inherited disorder characterized by diminished hormone production by the testes or ovaries (hypogonadism), progressive loss of vision (retinitis pigmentosa), mental retardation, ...

Laurence-Moon Syndrome ... reduced hormone production by testes
Leriche syndrome ... impotence
Leriche's Syndrome ... impotence
Leukemia ... swollen testicles
Leydig cells hypoplasia ... small penis
Leydig cells hypoplasia, type I ... small penis ...

Fenigidin, gamma-Carboxyglutamic Acid, Glycosyl Ceramidase, Guanosine Diphosphofucose, Hemlock Tree, Histocompatibility Testing, Hypochlorous Acids, Hypotension, Orthostatic, Implants, Artificial, Infrared Rays, L-735 524, Laurence-Moon Syndrome, ...

If a child has underlying health problems, including a syndrome that might affect growth (Down syndrome, Prader-Willi syndrome, Laurence-Moon syndrome, Bardet-Biedl syndrome, Turner syndrome, and certain other genetic conditions), ...

See also: Symptom, Retinitis pigmentosa, Diabetes, Dystrophy, Kidney

Disease Launois-Bensaude syndromeLaurence-moon-biedl syndrome

 
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