ライフサイエンスコーパス: hypertelorism

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1 ening between the eyes, a condition known as hypertelorism.

2 and prevalence of extra-aortic features (29% hypertelorism, 53% cervical arterial tortuosity, and 27%

3 ocular features were epicanthic folds (84%), hypertelorism (68%), ptosis (56%), high upper eyelid cre

4 crocephaly, prominent eyes, arched eyebrows, hypertelorism, a glabellar nevus flammeus, neonatal feed

5 rum ranges from cyclopia and hypotelorism to hypertelorism and facial duplications.

6 teins are candidates for human conditions of hypertelorism and FNDs.

7 cilia on cranial neural crest cells, causes hypertelorism and frontonasal dysplasia (FND).

8 (OS) is a congenital defect characterized by hypertelorism and hypospadias, but additional midline ma

9 triad of arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate and is ca

10 leptic susceptibility, frontal bossing, mild hypertelorism, and downslanting palpebral fissures.

11 males are usually more mildly affected with hypertelorism as the only feature.

12 frontal hairline, facial asymmetry, ptosis, hypertelorism, broad great toes, and clinodactyly.

13 n and digit duplications, atresia, fistulas, hypertelorism, cleft palate and hamartoma.

14 sign"), typical cranio-facial dysmorphisms (hypertelorism, depressed nasal bridge, frontal bossing),

15 h anterior hair line, broad medial eyebrows, hypertelorism, downslanted palpebral fissures, broad nas

16 ted events were macrocrania in six patients, hypertelorism in three patients, and multiple basal cell

17 Mild facial anomalies include hypertelorism, low-set ears, epicanthal folds and macrog

18 stic features include combinations of ocular hypertelorism, malformations of the nose and forehead an

19 bsence of flat bones within the skull vault, hypertelorism, open-bite malocclusion, cleft palate and

20 ypothalamic hamartoma and PHS does not cause hypertelorism or broadening of the nasal root or forehea

21 rdiographic conduction abnormalities, Ocular hypertelorism, Pulmonary stenosis, Abnormal genitalia, R

22 , electrocardiographic abnormalities, ocular hypertelorism, pulmonary valve stenosis, abnormal genita

23 nes, Electrocardiogram abnormalities, Ocular hypertelorism, Pulmonic valvular stenosis, Abnormalities

24 ers exhibited dysmorphic features, including hypertelorism, small mandible, syndactyly, clinodactyly,

25 defects, and dysmorphic facial features with hypertelorism, synophrys, macroglossia, protruding tongu

26 Distinctive facial features consisting of hypertelorism, telecanthus, blepharophimosis, blepharopt

27 zed by a distinctive facial appearance, with hypertelorism, wide nasal bridge, short nasal ridge, bif

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