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1 viduals, who had (relative) macrocephaly and hypertelorism.
2 ening between the eyes, a condition known as hypertelorism.
3 and prevalence of extra-aortic features (29% hypertelorism, 53% cervical arterial tortuosity, and 27%
4 ocular features were epicanthic folds (84%), hypertelorism (68%), ptosis (56%), high upper eyelid cre
5 cluded a prominent forehead, a flat midface, hypertelorism, a broad nose, downturned corners of mouth
6            This impacts our understanding of hypertelorism, a disorder associated with mutations in s
7 crocephaly, prominent eyes, arched eyebrows, hypertelorism, a glabellar nevus flammeus, neonatal feed
8 rum ranges from cyclopia and hypotelorism to hypertelorism and facial duplications.
9 teins are candidates for human conditions of hypertelorism and FNDs.
10  cilia on cranial neural crest cells, causes hypertelorism and frontonasal dysplasia (FND).
11 (OS) is a congenital defect characterized by hypertelorism and hypospadias, but additional midline ma
12  triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate and is ca
13 leptic susceptibility, frontal bossing, mild hypertelorism, and downslanting palpebral fissures.
14  males are usually more mildly affected with hypertelorism as the only feature.
15                                              Hypertelorism, bifid uvula, and arterial tortuosity appr
16  frontal hairline, facial asymmetry, ptosis, hypertelorism, broad great toes, and clinodactyly.
17 n and digit duplications, atresia, fistulas, hypertelorism, cleft palate and hamartoma.
18 ants show syndromic malformations, including hypertelorism, cleft palate and omphalocele.
19  sign"), typical cranio-facial dysmorphisms (hypertelorism, depressed nasal bridge, frontal bossing),
20 h anterior hair line, broad medial eyebrows, hypertelorism, downslanted palpebral fissures, broad nas
21 istinctive facial characteristics, including hypertelorism, epicanthal folds, blepharoptosis, a small
22 ted events were macrocrania in six patients, hypertelorism in three patients, and multiple basal cell
23                Mild facial anomalies include hypertelorism, low-set ears, epicanthal folds and macrog
24 stic features include combinations of ocular hypertelorism, malformations of the nose and forehead an
25 ures, and ocular alterations such as ptosis, hypertelorism, nystagmus, and chorioretinal coloboma.
26 bsence of flat bones within the skull vault, hypertelorism, open-bite malocclusion, cleft palate and
27 ypothalamic hamartoma and PHS does not cause hypertelorism or broadening of the nasal root or forehea
28 rdiographic conduction abnormalities, Ocular hypertelorism, Pulmonary stenosis, Abnormal genitalia, R
29 , electrocardiographic abnormalities, ocular hypertelorism, pulmonary valve stenosis, abnormal genita
30 nes, Electrocardiogram abnormalities, Ocular hypertelorism, Pulmonic valvular stenosis, Abnormalities
31 ects in eye development, prominent forehead, hypertelorism, short stature and brachydactyly, is cause
32 ers exhibited dysmorphic features, including hypertelorism, small mandible, syndactyly, clinodactyly,
33 defects, and dysmorphic facial features with hypertelorism, synophrys, macroglossia, protruding tongu
34    Distinctive facial features consisting of hypertelorism, telecanthus, blepharophimosis, blepharopt
35 zed by a distinctive facial appearance, with hypertelorism, wide nasal bridge, short nasal ridge, bif