Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type

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.

Also known as: Hadziselimovic syndrome, microcephaly-faciocardioskeletal syndrome

0 clinical trials for this condition and its sub-types, 0 tagged with Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type itself.