vitalwiki

Pfeiffer-Palm-Teller syndrome

ORPHA:2871· ICD-10 Q87.1

Definition

A rare multiple congenital anomalies/dysmorphic syndrome characterized by short stature, small hands and feet, stiff gait, slow movements, high-pitched voice and progressive joint stiffness, particularly in the shoulders, elbows, fingers and hands. Patients typically present with amimic facies with narrow palpebral fissures with epicanthal folds, cup-shaped ears, high-arched palate and enamel hypoplasia. Recurrent bronchitis is frequently observed. Inguinal hernia, clinodactyly and congenital aortic stenosis may also be present. There have been no further descriptions in the literature since 1977.

Prevalence
<1 / 1 000 000
Age of onset
Neonatal