Optimal surgical correction of the craniofacial manifestations of cleidocranial dysplasia
(CCD) has not been established due to the rarity of the condition. A 27-year-old female with …

Background: Cleidocranial dysostosis (CCD) is a rare genetic disease that compromises
normal bone development, caused by the alteration in the RUNX2 gene of chromosome 6p …

Background: Skeletal dysplasias encompass a group of genetic conditions associated with
cartilaginous and bone tissue abnormalities, exhibiting a variable phenotype depending on …

Sažetak Orofacijalni sindromi heterogena su skupina poremećaja koji imaju različito
izražene anomalije pogotovo kraniofacijalne, ali i drugih regija. S većim saznanjem o …

A male infant was delivered vaginally at 37+ 4 weeks after an uncomplicated pregnancy with
normal antenatal ultrasonography. An abnormal head shape was noted, with normal head …

Cleidocranial dysplasia (CCD) is a rare genetic skeletal syndrome. The most common
features are open fontanelles, hypertelorism, mid-face retrusion, hypoplasia, or aplasia of …

Cleidocranial dysplasia (CCD), also known as Marie-Sainton syndrome, is a rare disorder of
autosomal dominant type that presents specific characteristics at the skeletal and dental …

Hypophosphatasia (HPT) and cleidocranial dysplasia (CCD) are rare genetic disorders
characterized by both defective ossification and bone mineralization. Patients usually …

El hueso es un tipo de tejido conectivo especializado que proporciona sostén, protección y
homeostasis del calcio. Este tejido está compuesto de matriz extracelular y células. Se …

Some malformative diseases have a prevalent, although not exclusive, involvement of the
bones of the skull and face. The common pathogenetic moment is an anomalous closure of …