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Dictionary » Glucocerebrosidosis
 

Glucocerebrosidosis

Introduction: Glucocerebrosidosis

Description of Glucocerebrosidosis

Glucocerebrosidosis: An autosomal recessive disorder caused by deficiency of the enzyme glucocerebrosidase (see GLUCOSYLCERAMIDASE) featuring the pathological storage of glycosylceramide in mononuclear PHAGOCYTES (Gaucher Cells). The most common subtype is the non-neuronopathic form, a slowly progressive condition characterized by hepatosplenomegaly and skeletal deformities. The neuronopathic forms are divided into infantile and juvenile forms. The infantile form presents at 4-5 months of age with anemia, loss of cognitive gains, neck retraction, dysphagia, and hepatosplenomegaly. The juvenile form features a slowly progressive loss of intellect, hepatosplenomegaly, ATAXIA, myoclonic SEIZURES, and spasticity. The neuronopathic forms are characterized by neuronal loss with neuronophagia, and accumulation of glucocerebroside in neurons. (From Baillieres Clin Haematol 1997 Dec;10(4):711-23; Menkes, Textbook of Child Neurology, 5th ed, p97)
Source: Diseases Database

Glucocerebrosidosis: Related Topics

These medical condition or symptom topics may be relevant to medical information for Glucocerebrosidosis:

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Terms Similar to Glucocerebrosidosis:

Source: Diseases Database

The following terms can be used for Glucocerebrosidosis

Source: CRISP

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Source: Diseases Database

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