Genitopatellar syndrome (GPS) is a rare disorder characterized by patellar hypoplasia, flexion contractures of the lower limbs, psychomotor retardation and genital and renal anomalies. We report the case of a female infant diagnosed with GPS to a KAT6B gene mutation, which was identified using whole exome sequencing.ope
Background Gorlin–Chaudhry–Moss syndrome (GCMS) and Fontaine–Farriaux syndrome (FFS) are extremely ...
Walker Warburg syndrome (WWS) lies at the severe end of the spectrum of the congenital muscular dyst...
KBG syndrome is a rare neurodevelopmental disorder characterized by intellectual disability, skeleta...
Genitopatellar syndrome (GPS) is a rare disorder in which patellar aplasia or hypoplasia is associat...
Heterozygous pathogenic variants in the KAT6B gene, which encodes lysine acetyltransferase 6B, have ...
Genitopatellar syndrome (GPS) is a rare autosomal dominant disorder caused by de novo pathogenic var...
Item does not contain fulltextGenitopatellar syndrome (GPS) is a rare disorder in which patellar apl...
KAT6B sequence variants have been identified previously in both patients with the Say-Barber-Bieseck...
KAT6B sequence variants have been identified previously in both patients with the Say-Barber-Bieseck...
Say-Barber-Biesecker-Young-Simpson Syndrome (SBBYSS; OMIM 603736), which overlaps with the originall...
Genitopatellar syndrome (GPS) is a skeletal dysplasia with cerebral and genital anomalies for which ...
KAT6B sequence variants have been identified in both patients with the Say\ue2\u80\u93Barber\ue2\u80...
Purpose :Genitopatellar syndrome and Say–Barber–Biesecker–Young–Simpson syndrome are caused by varia...
Lethal neonatal rigidity and multifocal seizure syndrome (RMFSL) is a severe autosomal recessive epi...
KAT6A syndrome is an autosomal dominant genetic disorder associated with intellectual disability due...
Background Gorlin–Chaudhry–Moss syndrome (GCMS) and Fontaine–Farriaux syndrome (FFS) are extremely ...
Walker Warburg syndrome (WWS) lies at the severe end of the spectrum of the congenital muscular dyst...
KBG syndrome is a rare neurodevelopmental disorder characterized by intellectual disability, skeleta...
Genitopatellar syndrome (GPS) is a rare disorder in which patellar aplasia or hypoplasia is associat...
Heterozygous pathogenic variants in the KAT6B gene, which encodes lysine acetyltransferase 6B, have ...
Genitopatellar syndrome (GPS) is a rare autosomal dominant disorder caused by de novo pathogenic var...
Item does not contain fulltextGenitopatellar syndrome (GPS) is a rare disorder in which patellar apl...
KAT6B sequence variants have been identified previously in both patients with the Say-Barber-Bieseck...
KAT6B sequence variants have been identified previously in both patients with the Say-Barber-Bieseck...
Say-Barber-Biesecker-Young-Simpson Syndrome (SBBYSS; OMIM 603736), which overlaps with the originall...
Genitopatellar syndrome (GPS) is a skeletal dysplasia with cerebral and genital anomalies for which ...
KAT6B sequence variants have been identified in both patients with the Say\ue2\u80\u93Barber\ue2\u80...
Purpose :Genitopatellar syndrome and Say–Barber–Biesecker–Young–Simpson syndrome are caused by varia...
Lethal neonatal rigidity and multifocal seizure syndrome (RMFSL) is a severe autosomal recessive epi...
KAT6A syndrome is an autosomal dominant genetic disorder associated with intellectual disability due...
Background Gorlin–Chaudhry–Moss syndrome (GCMS) and Fontaine–Farriaux syndrome (FFS) are extremely ...
Walker Warburg syndrome (WWS) lies at the severe end of the spectrum of the congenital muscular dyst...
KBG syndrome is a rare neurodevelopmental disorder characterized by intellectual disability, skeleta...