Microcephaly-facio-cardio-skeletal syndrome, Hadziselimovic type is a malformation syndrome with cardiac malformations (see this term) characterized by prenatal onset growth retardation (low birth weight and short stature), hypotonia, developmental delay and intellectual disability associated with microcephaly, 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 (see these terms) and skeletal (hypoplastic thumbs and first metacarpals) abnormalities. The disease is Orphanet_217026 (Microcephaly - facio-cardio-skeletal syndrome, Hadziselimovic type). Also known as: Hadziselimovic syndrome.