COCKAYNE SYNDROME: REPORT OF TWO CASES WITHIN A FAMILY
The clinical and phenotypic features of two siblings (a 12 years old girl and her 7 year old brother) with Cockayne syndrome are described. The main problems were mild to moderate mental retardation, dwarfism, clumsy gait, photosensitive skin lesions and progeroid (senile like) appearance. Brain CT...
Main Author: | M. Mohammadi |
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Format: | Article |
Language: | English |
Published: |
Tehran University of Medical Sciences
1999-07-01
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Series: | Acta Medica Iranica |
Subjects: | |
Online Access: | http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/4859.pdf&manuscript_id=4859 |
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