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English Wikipedia
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lüll New developments in the management of Anderson-Fabry disease Mehta AQJM 2002[Oct]; 95 (10): 647-53Anderson-Fabry disease (AFD) is a rare, X-linked lysosomal storage disorder that leads to accumulation of globotriasylceramide throughout diverse cells, tissues and organs of the body. The disease usually presents in childhood, is progressive, and results in increasing disability and premature death. Female carriers tend to be less severely affected. AFD is difficult to diagnose because of its heterogeneous signs and symptoms. Awareness is low among health professionals, and diagnosis is typically delayed for several years after first presentation. Treatment was formerly entirely symptomatic, but enzyme replacement therapy has recently been licensed and management is evolving from genetic counselling and palliative care to early diagnosis and active intervention.|Adolescent[MESH]|Adult[MESH]|Child[MESH]|Diagnosis, Differential[MESH]|Disease Progression[MESH]|Fabry Disease/complications/diagnosis/*therapy[MESH]|Humans[MESH] |