RETT SYNDROME: REPORT OF THREE CASES

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NASSIRIAN A.

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Journal Paper

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Journal: Journal of Medical Council of Iran Year:2002 | Volume:19 | Issue:4 Page(s): 299-302

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Information Journal Paper

Title

RETT SYNDROME: REPORT OF THREE CASES

Author(s)

NASSIRIAN A. | Issue Writer Certificate

Keywords

RETT SYNDROMEQ4

NEURODEGENERATIVE DISEASESQ4

SEXLINKED DISEASESQ4

Abstract

RETT SYNDROME is a sexlinked neurodegenrative disorder causing disability and occurs only in young female children with unknown etiology. The disorder begins in the late infancy with regression of neurodevelopmental state and psycho-behavioral signs and symptoms such as autistic behaviour, hand wringing, speech regression, choreo-athetotic movements in limbs and trunk, spastic and ataxic gait, inability to walk and talk, demented state and severe deformity of the spine.In the past three years, three new cases of them were diagnosed and managed. In this article, we would describe in short the physiopathology, the clinical signs, the clinical course and the probable treatment modalities of this syndrome.

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APA: Copy

NASSIRIAN, A.. (2002). RETT SYNDROME: REPORT OF THREE CASES. JOURNAL OF MEDICAL COUNCIL OF I.R.I., 19(4), 299-302. SID. https://sid.ir/paper/41456/en

Vancouver: Copy

NASSIRIAN A.. RETT SYNDROME: REPORT OF THREE CASES. JOURNAL OF MEDICAL COUNCIL OF I.R.I.[Internet]. 2002;19(4):299-302. Available from: https://sid.ir/paper/41456/en

IEEE: Copy

A. NASSIRIAN, “RETT SYNDROME: REPORT OF THREE CASES,” JOURNAL OF MEDICAL COUNCIL OF I.R.I., vol. 19, no. 4, pp. 299–302, 2002, [Online]. Available: https://sid.ir/paper/41456/en

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