Diagnóstico clínico en el síndrome de Kabuki: fenotipo y anomalías asociadas en dos casos nuevos. / [Clinical diagnosis of Kabuki syndrome: phenotype and associated abnormalities in two new cases].
Arch Argent Pediatr
; 112(1): 26-32, 2014 Feb.
Article
in Es
| BINACIS
| ID: bin-133654
ABSTRACT
Kabuki syndrome is a genetic entity with multiple anomalies associated with intellectual disability. The clinical diagnosis is based on typical facial features, minor skeletal abnormalities, finger pads, and postnatal growth deficit. Other findings may include congenital heart disease, genitourinary anomalies, oral clefts, anal atresia, increased susceptibility to infections, autoimmune and endocrine disease and hearing loss. The objective of this paper is to describe two patients with clinical diagnosis of Kabuki syndrome, highlighting the phenotypic findings and associated malformations.
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Collection:
06-national
/
AR
Database:
BINACIS
Type of study:
Diagnostic_studies
/
Risk_factors_studies
Language:
Es
Journal:
Arch Argent Pediatr
Year:
2014
Document type:
Article
Country of publication:
Argentina