FABRY DISEASE (A KIND OF LYSOSOMAL STORAGE DISEASE)

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KARIMZADEH PARVANEH

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Journal Paper

Paper Information

Journal: Iranian Journal of Child Neurology Year:2012 | Volume:6 | Issue:4 (SUPPL 1) Page(s): 6-6

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Information Journal Paper

Title

FABRY DISEASE (A KIND OF LYSOSOMAL STORAGE DISEASE)

Author(s)

KARIMZADEH PARVANEH | Issue Writer Certificate

Keywords

FABRY DISEASE

CHILDHOOD

ENZYME REPLACEMENT THERAPY

Abstract

FABRY DISEASE is an X-linked disorder. This condition is an inherited disorder that begins in CHILDHOOD, causes signs and symptoms of many parts of body.Characteristic clinical features of disease, include episodes of pain, particularly in the hands and feet (acropares thesia), small dark red spots (on the skin) called angiokeratomas, decreases ability to sweat (hypohidrosis, crnealopacity, disorders in Gastrointestinal tract, ear ringing (tinnitus), Hearing impairment and nephrologic problem.

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APA: Copy

KARIMZADEH, PARVANEH. (2012). FABRY DISEASE (A KIND OF LYSOSOMAL STORAGE DISEASE). IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), 6(4 (SUPPL 1)), 6-6. SID. https://sid.ir/paper/303469/en

Vancouver: Copy

KARIMZADEH PARVANEH. FABRY DISEASE (A KIND OF LYSOSOMAL STORAGE DISEASE). IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN)[Internet]. 2012;6(4 (SUPPL 1)):6-6. Available from: https://sid.ir/paper/303469/en

IEEE: Copy

PARVANEH KARIMZADEH, “FABRY DISEASE (A KIND OF LYSOSOMAL STORAGE DISEASE),” IRANIAN JOURNAL OF CHILD NEUROLOGY (IJCN), vol. 6, no. 4 (SUPPL 1), pp. 6–6, 2012, [Online]. Available: https://sid.ir/paper/303469/en

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