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Results 1 - 10 of 111 for Death in childhood
  1. CLN1 disease 
    ... disease leads to severe signs and symptoms and death in childhood.In the later-onset cases of CLN1 disease, ... those who have the condition beginning in early childhood. As a result, ... and cause nerve cell death, the signs and symptoms of CLN1 disease in ...
    https://medlineplus.gov/genetics/condition/cln1-disease - Genetics
  2. X-linked hyper IgM syndrome 
    ... family. Without treatment, this condition can result in death during childhood or adolescence. X-linked hyper IgM syndrome is ...
    https://medlineplus.gov/.../condition/x-linked-hyper-igm-syndrome - Genetics
  3. Congenital bile acid synthesis defect type 1 
    ... defect type 1 often leads to cirrhosis and death in childhood. The prevalence of congenital bile acid synthesis defect ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-1 - Genetics
  4. Congenital bile acid synthesis defect type 2 
    ... defect type 2 typically leads to cirrhosis and death in childhood. The prevalence of congenital bile acid synthesis defect ...
    https://medlineplus.gov/...genital-bile-acid-synthesis-defect-type-2 - Genetics
  5. Hennekam syndrome 
    ... severity of the condition and can vary from death in childhood to survival into adulthood. At least 50 cases ...
    https://medlineplus.gov/genetics/condition/hennekam-syndrome - Genetics
  6. X-linked lymphoproliferative disease 
    ... treatment, most people with XLP survive only into childhood. Death usually results from hemophagocytic lymphohistiocytosis.XLP can be ...
    https://medlineplus.gov/.../x-linked-lymphoproliferative-disease - Genetics
  7. Glycogen storage disease type 0 
    ... and sudden death, particularly after physical activity. Sudden death from cardiac arrest can occur in childhood or adolescence in people with muscle GSD 0. ...
    https://medlineplus.gov/.../glycogen-storage-disease-type-0 - Genetics
  8. 15q11-q13 duplication syndrome 
    ... cases, sudden death during sleep (called sudden unexpected death in epilepsy, or SUDEP).Hearing loss in childhood is common in dup15q syndrome and usually results ...
    https://medlineplus.gov/.../condition/15q11-q13-duplication-syndrome - Genetics
  9. TK2-related mitochondrial DNA depletion syndrome, myopathic form 
    ... Respiratory failure is the most common cause of death in people with TK2-MDS, often occurring in childhood. Rarely, the disorder progresses slowly and affected individuals ...
    https://medlineplus.gov/...ial-dna-depletion-syndrome-myopathic-form - Genetics
  10. Sitosterolemia 
    ... chance of a heart attack, stroke, or sudden death.Some people with sitosterolemia develop small yellowish growths called xanthomas beginning in childhood. Xanthomas consist of accumulated lipids and may be ...
    https://medlineplus.gov/genetics/condition/sitosterolemia - Genetics
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