نتایج جستجو برای: facial
تعداد نتایج: 60417 فیلتر نتایج به سال:
background: 49, xxxxy syndrome is a rare sex chromosomal disorder, occurring in 1 per 85,000-100,000 male births. the classical phenotype is ambiguous genitalia, facial dysmorphism, mental retardation and a combination of cardiac, skeletal and other malformations. case: a two month-old boy with intrauterine growth restriction (iugr) and low birth weight, facial dysmorphism, clinodactyly in feet...
Background: Mycobacterium tuberculosis is a rare cause of mastoiditis, but diagnosis is often delayed, with potentially serious results. Case: We report a case of tuberculous mastoiditis with unilateral hearing loss, facial paralysis, and cervical lymph adenopathy on presentation. Conclusion: Tuberculous mastoiditis must be considered in all cases of chronic refractory m...
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