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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CONCLUSIONS
This report contributes to the clinical spectrum of
Wolf-Hirschhorn syndrome, from infant to young teenager,
including severe growth retardation, absence of speech and
friendly behavior, corresponding to the specific cytogenetic
anomalies. Concerning the particularities in this case
with a complex clinical aspect, from a cytogenetic point of
view, the karyotype had the cytogenetic formula in mosaic,
which has rarely been reported in literature. The severity
of the symptoms in mosaic Wolf-Hirschhorn may depend
on the amount of deletion, but more research is needed.
Moreover, this article presents, for the first time in
literature, the aspects of cephalometric analysis in a patient
with Wolf-Hirschhorn syndrome. Further studies are
necessary in order to clarify the pattern of craniofacial
development. In patients with Wolf-Hirschhorn syndrome,
cephalometric analysis can provide valuable information
about their craniofacial characteristics, which can be useful
in diagnosis, treatment planning and monitoring of the
condition over time.
Declaration of Patient Consent
The authors certify that informed consent was obtained
from the legal representative, before the beginning
of the study, for reporting images and clinical information
on the patient in the Journal.
Declaration of Interest
The authors report no conflicts of interest. The authors
alone are responsible for the content and writing of
this article.
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