Congenital anomalies · 2017
A Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome with a KAT6B 10-base pair palindromic duplication: A recurrent mutation causing a severe phenotype mixed with genitopatellar syndrome.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Niida Yo, Mitani Yusuke, Kuroda Mondo, Yokoi Ayano, Nakagawa Hiroyasu, Kato Akiko
Аннотация
The Say-Barber-Biesecker-Young-Simpson variant of Ohdo syndrome (SBBYSS) (MIM# 603736) and genitopatellar syndrome (GPS) (MIM#606170) are allelic diseases caused by KAT6B mutation. Genotype-phenotype correlation is assumed, but a few patients manifest overlapping features of both syndromes. Here we report the case of a boy with SBBYSS. He had a KAT6B mutation previously reported in typical SBBYSS, but he also manifested severe developmental delay, as well as genital features and laryngomalacia requiring tracheostomy that conformed to GPS.
Предметные рубрики MeSH
AllelesBlepharophimosisCongenital HypothyroidismCraniofacial AbnormalitiesDNA Mutational AnalysisDiagnosis, DifferentialExonsFaciesGene DuplicationGenetic Association StudiesHeart Defects, CongenitalHistone AcetyltransferasesHumansInfant, NewbornIntellectual DisabilityInverted Repeat SequencesJoint InstabilityKidneyMaleMutationPatellaPhenotypePsychomotor DisordersRadiographyScrotumUltrasonography, PrenatalUrogenital Abnormalities