| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Jennifer M Hendi, Robert Nemerofsky, Cynthia Stolman, Mark S Granic. Plastic surgery considerations for holoprosencephaly patients. The Journal of craniofacial surgery. vol 15. issue 4. 2004-10-19. PMID:15213551. |
holoprosencephaly (hpe) is considered the leading abnormality of the brain and face in humans and is frequently associated with a wide spectrum of specific craniofacial anomalies including mid-line facial clefts, cyclopia and nasal irregularities. |
2004-10-19 |
2023-08-12 |
Not clear |
| Peter J Taub, James P Bradley, Bernard L Markowit. Single-stage lip and nasal reconstruction in holoprosencephaly. Plastic and reconstructive surgery. vol 111. issue 7. 2003-07-23. PMID:12794475. |
single-stage lip and nasal reconstruction in holoprosencephaly. |
2003-07-23 |
2023-08-12 |
Not clear |
| F V Mehendale, B C Sommerla. Airway obstruction due to a rudimentary premaxilla in holoprosencephaly. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. vol 38. issue 3. 2001-10-04. PMID:11386438. |
we present two infants with holoprosencephaly and clefts of the primary palate, who developed nasal airway obstruction due to a previously undocumented cause: a ball-valve-like action of a rudimentary premaxilla, which was extremely mobile on a soft tissue stalk. |
2001-10-04 |
2023-08-12 |
Not clear |
| B D Vanzieleghem, M M Lemmerling, H F Vermeersch, P Govaert, I Dhooge, F Meire, G R Mortier, J Leroy, M F Kunne. Imaging studies in the diagnostic workup of neonatal nasal obstruction. Journal of computer assisted tomography. vol 25. issue 4. 2001-08-09. PMID:11473183. |
four groups were recognized: group i: choanal atresia (n = 5) and choanal stenosis (n = 1); group ii: congenital nasal pyriform aperture stenosis (cnpas) (n = 3) and holoprosencephaly (n = 1); group iii: nasolacrimal duct mucocele (n = 1); group iv: nasal hypoplasia (n = 1). |
2001-08-09 |
2023-08-12 |
Not clear |
| M A Godil, P Galvin-Parton, D Monte, M Zerah, A Purandare, A H Lane, T A Wilso. Congenital nasal pyriform aperture stenosis associated with central diabetes insipidus. The Journal of pediatrics. vol 137. issue 2. 2000-09-19. PMID:10931423. |
this association further strengthens the concept that congenital nasal pyriform aperture stenosis may be a microform of holoprosencephaly. |
2000-09-19 |
2023-08-12 |
Not clear |
| R A Martin, K L Jone. Absence of the superior labial frenulum in holoprosencephaly: a new diagnostic sign. The Journal of pediatrics. vol 133. issue 1. 1998-07-29. PMID:9672532. |
absence of the frenulum in holoprosencephaly also provides evidence that its embryonic origin is that of the medial nasal process. |
1998-07-29 |
2023-08-12 |
Not clear |
| B J Krol, G F Hulka, A Drak. Congenital nasal pyriform aperture stenosis in the monozygotic twin of a child with holoprosencephaly. Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery. vol 118. issue 5. 1998-06-02. PMID:9591870. |
congenital nasal pyriform aperture stenosis in the monozygotic twin of a child with holoprosencephaly. |
1998-06-02 |
2023-08-12 |
Not clear |
| F S Lo, Y J Lee, S P Lin, E Y Shen, J K Huang, K S Le. Solitary maxillary central incisor and congenital nasal pyriform aperture stenosis. European journal of pediatrics. vol 157. issue 1. 1998-03-17. PMID:9461361. |
solitary maxillary central incisor (smci) and congenital nasal pyriform aperture stenosis (cnpas) have been reported as an isolated morphogenic defect or associated with pituitary deficiency, holoprosencephaly, ocular coloboma, or chromosomal abnormalities. |
1998-03-17 |
2023-08-12 |
Not clear |
| Y Yonehara, T Takato, T Komor. A unilateral cleft lip patient with holoprosencephaly. Annals of plastic surgery. vol 39. issue 2. 1997-10-10. PMID:9262780. |
holoprosencephaly includes a spectrum of conditions that have in common the associated anomalies of false median cleft lip, nasal malformation, orbital hypotelorism, and brain malformations. |
1997-10-10 |
2023-08-12 |
Not clear |
| M Galguera, L Malave, A Leo. Holoprosencephaly with proboscis. Gynecologic and obstetric investigation. vol 42. issue 1. 1996-12-12. PMID:8840183. |
this is the case of a male newborn with holoprosencephaly, marked hypotelorism, and a rudimentary nasal structure, the proboscis. |
1996-12-12 |
2023-08-12 |
Not clear |
| S R Braddock, M R Grafe, K L Jone. Development of the olfactory nerve: its relationship to the craniofacies. Teratology. vol 51. issue 4. 1995-11-14. PMID:7570367. |
although absence of the olfactory bulbs is a relatively common occurrence seen in holoprosencephaly, in kallman syndrome, and in a number of malformation syndromes, the extent to which it determines olfactory nerve development, as well as the part it plays in the morphogenesis of the nasal structures, is unknown. |
1995-11-14 |
2023-08-12 |
Not clear |
| Y Hui, J Friedberg, W S Crysdal. Congenital nasal pyriform aperture stenosis as a presenting feature of holoprosencephaly. International journal of pediatric otorhinolaryngology. vol 31. issue 2-3. 1995-07-20. PMID:7782184. |
congenital nasal pyriform aperture stenosis as a presenting feature of holoprosencephaly. |
1995-07-20 |
2023-08-12 |
Not clear |
| G S LaTrenta, H W Choi, R F Ward, L Hoffman, J A Neidic. Complete nasal agenesis with bilateral microphthalmia and unilateral duplication of the thumb. Plastic and reconstructive surgery. vol 95. issue 6. 1995-06-01. PMID:7732122. |
complete nasal aplasia is an extremely rare clinical entity and most infants are stillborn when this is associated with holoprosencephaly. |
1995-06-01 |
2023-08-12 |
Not clear |
| S Durmuş Aydoğdu, A Yakut, U Oner, M A Akşit, N Te. Holoprosencephaly anomaly with nasal and premaxillar agenesis (possibly autosomal recessive type). The Turkish journal of pediatrics. vol 36. issue 2. 1994-07-26. PMID:8016918. |
holoprosencephaly anomaly with nasal and premaxillar agenesis (possibly autosomal recessive type). |
1994-07-26 |
2023-08-12 |
Not clear |
| E Tavin, E Stecker, R Mario. Nasal pyriform aperture stenosis and the holoprosencephaly spectrum. International journal of pediatric otorhinolaryngology. vol 28. issue 2-3. 1994-05-19. PMID:8157419. |
nasal pyriform aperture stenosis and the holoprosencephaly spectrum. |
1994-05-19 |
2023-08-12 |
Not clear |
| R C Hennekam, G Van Noort, F A de la Fuente, O F Norbrui. Agenesis of the nasal septal cartilage: another sign in autosomal dominant holoprosencephaly. American journal of medical genetics. vol 39. issue 1. 1991-09-12. PMID:1844347. |
agenesis of the nasal septal cartilage: another sign in autosomal dominant holoprosencephaly. |
1991-09-12 |
2023-08-11 |
Not clear |
| J L Spolyar, F Eldis, D Benjamin. Five cases of DeMyer sequence: an interophthalmic dysplasia. The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association. vol 28. issue 1. 1991-04-25. PMID:2004088. |
an intact ethmoid, nasal bone, and crista galli appear to represent key anatomic differences in these patients as compared to classical holoprosencephaly sequence subjects. |
1991-04-25 |
2023-08-11 |
human |
| S H Lieuw Kie Song, W Bee. Median facio-cerebral anomalies in chick embryos resulting from local destruction of the anteriormost parts of the early neural plate and neural crest. Acta morphologica Neerlando-Scandinavica. vol 18. issue 3. 1980-11-24. PMID:7415879. |
these anomalies included arhinencephaly, holoprosencephaly, anophthalmia, synophthalmia, microphthalmia, absence or reduction of the nasal structures, sometimes combined with the presence of a proboscis, and incidentally occurring facial cleft conditions. |
1980-11-24 |
2023-08-12 |
chicken |