Decreased width of the forehead. OMIM is intended for use primarily by physicians and other professionals concerned with genetic disorders, by genetics researchers, and by advanced students in science and medicine. We discuss possible genetic mechanisms underlying the complex pattern of inheritance for this condition. The etiology of her pattern of malformation was not identified at that time. Other features of the syndrome include malformed ears, unusual hair patterns on the scalp, bent fingers and toes and joint deformities in the hands and feet, unusual teeth, mild developmental delay , cryptorchidism , and a generally happy disposition. Genetic disorder stubs Genetic disorders by inheritance Rare syndromes. Disease definition The 8q
Nablus mask-like facial syndrome
OMIM Entry - # - NABLUS MASK-LIKE FACIAL SYNDROME; NMLFS
Description: Information in Orphanet is not intended to replace professional health care. The affected child appeared unusual at birth, whereas his twin sister appeared normal. Other parts of the body including skin, nails, and genitalia are unremarkable. The Orphanet rare disease nomenclature is comprised of a heterogeneous typology of entities of decreasing extension, including: He had an unaffected twin sister and healthy, non-consanguineous parents.