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"Prader-Willi" syndrome
- Prader-Willi syndrome is a disease that is present from birth (congenital). It affects many parts of the body. ... Prader-Willi syndrome is caused by a missing gene on chromosome 15. Normally, parents each pass down a copy ...
- ... be linked to rare genetic conditions, such as Prader-Willi syndrome . Prader-Willi syndrome is a disease that is present from birth ( ...
- ... eye during infancy Incontinentia pigmenti syndrome Noonan syndrome Prader-Willi syndrome Retinopathy of prematurity Retinoblastoma Traumatic brain injury Trisomy ...
- ... Obesity Genetic diseases, such as Klinefelter syndrome or Prader-Willi syndrome Other diseases, such as cystic fibrosis The following ...
- ... occurs with: Acromegaly Amyloidosis Down syndrome Myxedema Rhabdomyoma Prader Willi Syndrome Tongue cancer The tongue may get wider in ...
- ... nerve damage include: Down syndrome Spinal muscular atrophy Prader-Willi syndrome Tay-Sachs disease Trisomy 13 Other disorders that ...
- ... pituitary apoplexy , subarachnoid hemorrhage Genetic disorders, such as Prader-Willi syndrome , familial diabetes insipidus , Kallmann syndrome Infections and swelling ( ...