A very rare case of a newborn with tetrasomy 9p and literature review

Background. Tetrasomy 9p is a rare genetic condition which usually results from a supernumerary isochromosome derived from the short arm of chromosome 9. Phenotypic findings include multiple congenital anomalies, facial dysmorphism, growth and developmental delays, and also vary according to...

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Bibliographic Details
Main Authors: Merve Süleyman, Sümeyra Oğuz, Gözdem Kaykı, Hasan Tolga Çelik, Pelin Özlem Şimsek-Kiper, Gülen Eda Utine, Şule Yiğit
Format: Article
Language:English
Published: Hacettepe University Institute of Child Health 2022-02-01
Series:The Turkish Journal of Pediatrics
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Online Access:https://turkjpediatr.org/article/view/139
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