Single-stage lip and nasal reconstruction in holoprosencephaly

Plastic and Reconstructive Surgery

Volumn 111, Issue 7, 2003, Pages 2324-2327

  Taub, Peter J ^a   Bradley, James P ^a   Markowitz, Bernard L ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CASE REPORT; CLEFT LIP PALATE; CLINICAL FEATURE; DIAPHRAGM HERNIA; HOLOPROSENCEPHALY; HUMAN; HYPERTELORISM; HYPOPITUITARISM; LIP RECONSTRUCTION; MALE; MICROPENIS; NOSE MALFORMATION; NOSE RECONSTRUCTION; PRESCHOOL CHILD; PRIORITY JOURNAL; STOMACH FUNDOPLICATION; SURGICAL TECHNIQUE; TREATMENT OUTCOME;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; CLEFT LIP; CLEFT PALATE; HOLOPROSENCEPHALY; HUMANS; MALE; NOSE; RHINOPLASTY; SURGICAL FLAPS; SUTURE TECHNIQUES;

EID: 0037981612     PISSN: 00321052     EISSN: None     Source Type: Journal    
DOI: 10.1097/01.PRS.0000061060.47278.52     Document Type: Article

References (11)

1. Sadove, A. M., Eppley, B. L., and DeMeyer, W. Single stage repair of the median cleft lip deformity in holoprosencephaly. J. Craniomaxillofac. Surg. 17: 363, 1989.
2. Siebert, J. R., Kokich, V. G., Beckwith, J. B., Cohen, M. M., Jr., and Lemire, R. J. The facial features of holoprosencephaly in anencephalic human specimens: II. Craniofacial anatomy. Teratology 23: 305, 1981.
3. Cohen, M. M., Jr. An update on the holoprosencephalic disorders. J. Pediatr. 101: 865, 1982.
4. Olsen, C. L., Hughs, J. P., Youngblood, L. G., and Sharpe-Stimac, M. Epidemiology of holoprosencephaly and phenotypic characteristics of affected children: New York State, 1984-1989. Am. J. Med. Genet. 73: 217, 1997.
5. Roessler, E., Belloni, E., Gaudenz, K., et al. Mutations in the human Sonic Hedgehog cause holoprosencephaly. Nat. Genet. 14: 357, 1996.
6. Brown, S. A., Warburton, D., Brown, L. Y., et al. Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired. Nat. Genet. 20: 180, 1998.
7. Kawakami, K, Ohto, H., Takizawa, T., and Saito, T. Identification and expression of six family genes in mouse retina. FEBS Lett. 393: 259, 1996.
8. Gripp, K. W., Wotton, D., Edwards, M. C., et al. Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination. Nat. Genet. 25: 208, 2000.
9. Elias, D. L., Kawamoto, H. K., Jr., and Wilson, L. F. Holoprosencephaly and midline facial anomalies: Redefining classification and management. Plast. Reconstr. Surg. 90: 951, 1992.
10. DeMeyer, W., Zeman, W., and Palmer, C. G. The face predicts the brain: Diagnostic significance of median facial anomalies for holoprosencephaly (arhinencephaly). Pediatrics 34: 256, 1964.
11. Beasley, J. W., and Gregg, J. B. Single stage repair of a medial cleft lip in an infant with premaxillary agenesis. J. South Dakota State Med. Assoc. 24: 15, 1971.