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Type A Niemann-Pick is a severe neurologic disease, which generally leads to death by 2 to 3 years of age. In contrast, patients with type B generally have little or no neurologic involvement and may survive into late childhood or adulthood.

The underlying reason for this dramatic difference in the two forms of the disease is not really understood, and, at present, it is not possible to accurately predict the severity of the disease by enzyme testing.

A child showing signs of type C before 1 year of age may not live to school age. Children showing symptoms after entering school may live into their mid to late teens, with few surviving into their 20s.



Complications:
  • Damage to the brain with varying degrees of mental retardation and delayed development of physical skills
  • Blindness
  • Deafness
  • Progressive deterioration in conditon (this is a fatal disorder)


Calling your health care provider:
Text Continues Below



Call for an appointment with your health care provider and genetic counselor if you have a family history of this disorder and you plan to have children. Consider calling your health care provider if your child has feeding problems, does not seem to be developing properly, or is not gaining weight properly.




A.D.A.M., Inc. is accredited by URAC, also known as the American Accreditation HealthCare Commission (www.urac.org).

The information provided herein should not be used during any medical emergency or for the diagnosis or treatment of any medical condition. A licensed physician should be consulted for diagnosis and treatment of any and all medical conditions. Call 911 for all medical emergencies. Links to other sites are provided for information only -- they do not constitute endorsements of those other sites. Copyright 2004 A.D.A.M., Inc. Any duplication or distribution of the information contained herein is strictly prohibited.

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