NIEMANN PICK TYPE A, A CASE REPORT

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MOJTAHEDZADEH F.; GHASEMI M.

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Journal Paper

Paper Information

Journal: JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES Year:2006 | Volume:16 | Issue:53 Page(s): 112-118

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Information Journal Paper

Title

NIEMANN PICK TYPE A, A CASE REPORT

Author(s)

MOJTAHEDZADEH F. | GHASEMI M. | Issue Writer Certificate

Keywords

METABOLIC DISORDCRSQ2

SPHINGOLIPIDOSESQ3

NIEMANN PICK AQ3

Abstract

Niemann Pick type A is a very rare hereditary disease with an incidence 1 in 20000-40000 live birth, which is calassified as a shingolipidoses. The disease is marked by the abnormal accumulation of sphingomyelin in most tissues, secondary to sphingomylinase deficiency. The most clinical manifestations are: Splenohepatomegaly–cherry red maculae-neuropathologic findings . This is a case report of an infant with clinical manifestation of Niemann Pick disease type A.

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APA: Copy

MOJTAHEDZADEH, F., & GHASEMI, M.. (2006). NIEMANN PICK TYPE A, A CASE REPORT. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, 16(53), 112-118. SID. https://sid.ir/paper/45885/en

Vancouver: Copy

MOJTAHEDZADEH F., GHASEMI M.. NIEMANN PICK TYPE A, A CASE REPORT. JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES[Internet]. 2006;16(53):112-118. Available from: https://sid.ir/paper/45885/en

IEEE: Copy

F. MOJTAHEDZADEH, and M. GHASEMI, “NIEMANN PICK TYPE A, A CASE REPORT,” JOURNAL OF MAZANDARAN UNIVERSITY OF MEDICAL SCIENCES, vol. 16, no. 53, pp. 112–118, 2006, [Online]. Available: https://sid.ir/paper/45885/en

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