Moynahan syndrome (xte; xeroderma, talipes, and enamel defect)

General: Autosomal dominant inheritance; xeroderma, talipes, and enamel defect 626c24g .

Ocular: Absence of eyelashes of lower lid.

Clinical: Cleft palate; hypohidrosis; defective enamel; nail anomalies; coarse and dry hair; short-lasting skin bullae.

Magalini SI, Scrascia E. Dictionary of Medical Syndromes, 2nd ed. Philadelphia: JB Lippincott, 1981.

Moynahan E. XTE (xeroderma, talipes and enamel defect): a new heredo-familial syndrome. Two cases. Homozygous inheritance of a dominant gene. Proc R Soc Med 1970; 63:447-448.