American journal of medical genetics · 1995
Kabuki make-up (Niikawa-Kuroki) syndrome in five Spanish children.
Клинический случайСтатьяПоддержка исследования: вне правительства СШАОбзорНазвание и аннотация: Перевод в очереди
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Galán-Gómez E, Cardesa-García J J, Campo-Sampedro F M, Salamanca-Maesso C, Martínez-Frías M L, Frías J L
Аннотация
We describe 5 Spanish children with Kabuki make-up syndrome (KMS)-3 females and 2 males-identified in Badajoz, Spain, between 1988 and 1990. All had the characteristic clinical and radiological manifestations of the syndrome. Psychomotor/mental retardation, postnatal growth deficiency, distinctive facial appearance, sagittal vertebral clefts, and dermatoglyphic abnormalities were present in all 5. Congenital heart defects were present in 4 patients. In addition, one had myopia, astigmatism, and bilateral paralysis of the VI cranial nerve. Another had apparent fusion of the hamate and capitate. An additional patient, as well as his mother, had an apparently balanced 15/17 translocation [46,XY,t(15;17) (15q;21q)]. The fact that these patients were ascertained in a catchment area of approximately 250,000 inhabitants and in a relatively limited period of time suggests that the prevalence of the KMS may be higher than previously recognized.
Предметные рубрики MeSH
Abnormalities, MultipleAdultCatchment Area, HealthChild, PreschoolChromosome AberrationsChromosome DisordersChromosomes, Human, Pair 15Chromosomes, Human, Pair 17DermatoglyphicsFaceFemaleHand Deformities, CongenitalHeart Defects, CongenitalHumansInfant, NewbornIntellectual DisabilityMaleMiddle AgedPedigreePrevalenceSpainSyndromeTranslocation, Genetic