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Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2023

Potential benefit of rapid genetic testing for Pallister-Hall syndrome.

Клинический случайСтатьяНазвание и аннотация: Перевод в очереди
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Maeda-Usui Ayaka, Sato Takeshi, Nakano Satsuki, Kusakawa Moe, Kin Takane, Takahashi Nobuhiro, Motojima Yukiko, Asanuma Hiroshi, Hida Mariko, Ishii Tomohiro, Kuroda Tatsuo, Hasegawa Tomonobu

Аннотация

Pallister-Hall syndrome (PHS) is defined as a group of characteristic manifestations caused by a monoallelic GLI3 pathogenic variant. A two-month-old infant was referred to our institution because of undetermined sex. The infant had atypical genitalia with postaxial polysyndactyly, a hypothalamic mass, and an imperforate anus. We identified a known pathogenic variant of the GLI3 gene within one week and diagnosed the infant with PHS. The parents assigned the infant as male, considering the 46,XY karyotype, normal testosterone secretion, possible male identity, and the natural history of PHS. In infants with atypical genitalia and other malformations, such as polydactyly, a hypothalamic mass, or an imperforate anus, rapid GLI3 testing may provide information for planning lifelong management, including sex assignment.