Definition:
Hallerman-Streiff syndrome is a genetic defect characterized by malformations in the craniofacial area, ocular abnormalities, dental deformities, skin atrophy and short stature.
Diagnosis:
Hallermann-Streff syndrome can be diagnosed by the studying the characteristic features exhibited by the patient.
Treatment:
There is no treatment available for the condition.
Symptoms and Signs:
Among the characteristic features of people affected by the disorder are a short, broad head, underdeveloped mandible, arched palate and a thin, tapering nose. Congenital cataracts are also present.
Causes:
The condition is usually caused by genetic mutations that affect chromosomes responsible for muscoskeletal formation.
