منابع مشابه
Williams Syndrome with a “Twist”
Williams syndrome is a rare genetic condition with multisystemic involvement, caused by a microscopic deletion in the chromosome band 7q11.23. We describe the first case of a toddler with Williams syndrome who developed Benign Paroxysmal Torticollis (BPT), a benign dystonic disorder of unknown aetiology.
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ژورنال
عنوان ژورنال: Science
سال: 1901
ISSN: 0036-8075,1095-9203
DOI: 10.1126/science.13.314.36