FEATURES OF THE WOLF-HIRSCHHORN SYNDROME (WHS) FROM INFANT TO YOUNG TEENAGER
Popescu D.E., Marian D., Zeleniuc M., Samoila Ch., Belengeanu V.
*Corresponding Author: Corresponding Author: Marian Diana, DMD, PhD, Ass. Prof, Department of Operative Dentistry, Faculty of Dental Medicine, “Vasile Goldiş” Western University of Arad, Liviu Rebreanu St, no.86, 310414 Arad, Romania; tel.: 0040744187899, e-mail: marian.diana@uvvg.ro
page: 75
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Abstract
Wolf-Hirschhorn syndrome is a rare condition caused
by terminal deletions, of variable size, in the short arm of
chromosome 4. The syndrome displays the combination
of typical morphological facial variations, intellectual disability,
language delay, and various malformations. This
report describes the clinical aspect and developmental
evolution of a male patient with Wolf-Hirschhorn syndrome,
from infancy to adolescence. The patient was first
examined and diagnosed at 11 months, with follow-up at
the ages of 4 and 16.
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