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Chromosomal and clinical features in an infant with Hallermann-Streiff syndrome
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Editor,—Hallermann-Streiff syndrome (HSS) is a disorder of unknown origin rarely diagnosed in neonatal period. The early diagnosis of HSS is important for management because many complications, that are often life threatening, may occur early in this syndrome.1 We report an infant with clinical and radiological findings of HSS, a spontaneous fracture of the left arm, and with chromosome variant 46, XX, 16qh+. She was a girl born at term after …