New syndrome of skeletal, dental and hair anomalies.

Abstract

A Brother and sister are presented with the following abnormalities: dolichocephaly with tendency toward premature closure of the sagittal suture; antimongoloid slant of the eyes with epicanthal folds, full cheeks, everted lip, multiple oral frenula, mildly high-arched palate, and microdontia with possible enamel defect; posteriorly rotated low-set pinnae with deficient cartilage; a small short thorax with pectus excavatum; unusual dermatoglyphics, and abnormal hair growth and stucture; disproportionate shortening of the fibulae and the middle and distal phalanges of the toes and fingers; and somewhat flattened epiphyses. A paternal aunt gave birth to a stillborn dwarfed male with some of the same clinical features. Although an autopsy was obtained, unfortunately no roentgenograms were made.

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@article{Sensenbrenner1975NewSO, title={New syndrome of skeletal, dental and hair anomalies.}, author={Judith A Sensenbrenner and John P Dorst and Ruth P Owens}, journal={Birth defects original article series}, year={1975}, volume={11 2}, pages={372-9} }