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...
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| Format: | Article |
| Language: | English |
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Tehran University of Medical Sciences
1999-07-01
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| Series: | Acta Medica Iranica |
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| Online Access: | http://journals.tums.ac.ir/PdfMed.aspx?pdf_med=/upload_files/pdf/4859.pdf&manuscript_id=4859 |