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These helmets are used to treat deformational plagiocephaly, brachycephaly, scaphocephaly and other head shape deformities in infants 3–18 months of age by gently allowing the head shape to grow back into a normal shape. This type of treatment has been used for severe deformations.
Muenke syndrome: coronal craniosynostosis (plagiocephaly and brachycephaly), short feet and palms, hearing impairment, hypertelorism, and proptosis. [ 25 ] Pfeiffer syndrome : abnormalities of the skull, hands, and feet; wide-set, bulging eyes, an underdeveloped upper jaw, beaked nose.
Brachycephaly [51] Craniorhiny: Oxycephaly/turricephaly [52] Craniosynostosis, Boston type Coronal Brachycephaly, brachyturricephaly, trigonocephaly, turricephaly Usually considered nonsyndromic. [53] Craniosynostosis Susceptible cause; usually considered nonsyndromic. [54] Craniosynstosis Brachycephaly, plagiocephaly, turricephaly
Craniofacial surgery is a surgical subspecialty that deals with congenital and acquired deformities of the head, skull, face, neck, jaws and associated structures. Although craniofacial treatment often involves manipulation of bone, craniofacial surgery is not tissue-specific; craniofacial surgeons deal with bone, skin, nerve, muscle, teeth, and other related anatomy.
Cranial sutures. A defining characteristic of Crouzon syndrome is craniosynostosis, which results in an abnormal head shape.This is present in combinations of: frontal bossing, trigonocephaly (fusion of the metopic suture), brachycephaly (fusion of the coronal suture), dolichocephaly (fusion of the sagittal suture), plagiocephaly (unilateral premature closure of lambdoid and coronal sutures ...
While treatment is often as simply as repositioning the baby during sleep, in more pronounced cases helmet therapy may be put to use. In most cases, plagiocephaly is quite minor and easily resolved, with many more pediatric plastic surgeons becoming familiar with helmet therapy for more advanced cases. [7]
Antley–Bixler syndrome presents itself at birth or prenatally. [2] Features of the disorder include brachycephaly (flat forehead), craniosynostosis (complete skull-joint closure) of both coronal and lambdoid sutures, facial hypoplasia (underdevelopment); bowed ulna (forearm bone) and femur (thigh bone), synostosis of the radius (forearm bone), humerus (upper arm bone) and trapezoid (hand ...
The primary characteristics of FTHS are brachycephaly (flat head), wide fontanelle (soft spot on a baby's head), prominent forehead, hypertelorism (abnormally wide distance between the eyes), prominent eyes, macrocornea (large corneas), optic disc edema, full cheeks, small chin, bowing of the long bones in the arms or legs, and finger deformities.