Acrofacial dysostosis, Kennedy-Teebi type is a rare condition that affects the face and limbs. It is characterized by features such as a small head (microcephaly), narrow eye openings (blepharophimosis), small ears (microtia), a beaked nose, and the presence of cleft lip and/or palate. In addition, people with this condition may have similar changes in the thumbs and great toes and show signs of developmental delay. These features distinguish this disorder from other similar conditions, and although some of the characteristics have been noted in Nager syndrome, they appear in a specific pattern in acrofacial dysostosis, Kennedy-Teebi type. This summary is based on reported observations, and further research may help clarify the overlap between these conditions.

Common symptoms include a smaller than normal head, narrow openings of the eyelids, small ears, a beaked nose, and cleft lip and/or palate. In addition, the thumbs and great toes tend to be affected symmetrically. Developmental delays have also been observed in people with this condition.

Information about causes, genetics, and risk factors is currently limited for this condition.