A new familial syndrome characterized by pigmentary retinopathy, hypogonadism, mental retardation, nerve deafness and glucose intolerance. [electronic resource]
Producer: 19760423Description: 23-32 p. digitalISSN:- 0002-9343
- Adolescent
- Adrenal Glands -- physiopathology
- Adult
- Deafness -- genetics
- Diagnosis, Differential
- Female
- Follicle Stimulating Hormone -- blood
- Genes, Recessive
- Glucose -- metabolism
- Growth Hormone -- blood
- Humans
- Hypogonadism -- genetics
- Insulin -- blood
- Intellectual Disability -- genetics
- Laurence-Moon Syndrome -- diagnosis
- Luteinizing Hormone -- blood
- Male
- Pedigree
- Pituitary Gland -- physiopathology
- Retinitis Pigmentosa -- genetics
- Syndrome
- Testis -- physiopathology
- Thyroid Gland -- physiopathology
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Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.
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