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Watson syndrome
atypical form of neurofibromatois-1
Genetics:
- associated with mutation in gene for neurofibromin
Clinical manifestations:
- short stature
- macrocephaly
- lisch nodules
- pulmonic stenosis
- cafe-au-lait spots
- neurofibromas
Related
neurofibromatosis type 1 [NF1] protein or neurofibromin
General
neurofibromatosis (classic) type 1
Properties
ASSOCIATED-NEOPLASM[S]: pheochromocytoma
meningioma
glial neoplasm (glioma)
:SITE optic nerve (CN II, ON)
vestibular schwannoma
neurofibroma
malignant nerve sheath tumor
rhabdomyosarcoma
carcinoid
:SITE duodenum
parathyroid adenoma
Database Correlations
OMIM correlations