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Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type

ORPHA:217026· ICD-10 Q87.8

Definition

Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a rare syndrome with cardiac malformations, characterized by prenatal-onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly and craniofacial (low anterior hairline, hypotelorism, thick lips with carp-shaped mouth, high-arched palate, low-set ears), cardiac (conotruncal heart malformations such as tetralogy of Fallot) and skeletal (hypoplastic thumbs and first metacarpals) abnormalities.

Prevalence
<1 / 1 000 000
Inheritance
Unknown
Age of onset
Infancy, Neonatal