Valdés OJI

Language: English
References: 16
Page: 29-30
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Holoprosencephaly (HPE) is the most common structural anomaly of the development of human's forebrain, resulting from incomplete midline cleavage of the prosencephalon, associated with neurologic impairment and dysmorphism of the brain and face, due to disturbance of the delicate balance of signals required for proper separation of the cerebral hemispheres.

REFERENCES

1. 1.- Raam MS, Solomon BD, Muenke M. Holoprocencephaly: A Guide to Diagnosis and Clinical Management. Indian Pediatr. 2011;48(6):457-66.

2. 2.- Kauvar EF, Muen ke M. Holoprosen cephaly: recommendations for diagnosis and management. Curr Opin Pediatr. 2010;22(6):687-95.

3. 3.- OrioliIM, Castilla EE. Epidemiology of holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010;154C:13-21.

4. 4.- Leoncini E, Baranello G, Orioli IM, Annerén G, Bakker M, Bianchi F, et al. Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surceillance systems: searching for population variations. Birth Defects Res A. 2008;82:585-91.

5. 5.- Orioli IM, Amar E, Bakker MK, Bermejo-Sánchez E, Bianchi F, Canfield MA, Clementi M, Correa A, Csáky- Szunyogh M, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, Morgan M, Mutchinick OM, Rissmann A, Ritvanen A, Scarano G, Szabova E, Castilla EE. Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research. Am J Med Genet C Semin Med Genet. 2011;157C(4):344-57.

6. 6.- Sánchez J, Carstens E, Gutierrez J, Dezerga V, Sepúlveda W. Holoprocencefalia: Diagnóstico prenatal ultrasonográfico y manejo. Rev Chil Ultrasonog. 1998;1(4):120-23.

7. 7.- Saldarriaga W, Isaza C, Mastroiacovo P, Castilla EE. Cyclopia: a report of 4 cases born during a 170-day period in the Valle teaching hospital in Cali, Colombia. Rev Colomb Obstet Ginecol. 2007;58(1):70-7.

8. 8.- Poenaru MO, VilceaI D, Marin A. Holoprosencephaly:twocase reports. Maedica (Buchar). 2012;7(1):58-62.

9. 1.- Raam MS, Solomon BD, Muenke M. Holoprocencephaly: A Guide to Diagnosis and Clinical Management. Indian Pediatr. 2011;48(6):457-66.

10. 2.- Kauvar EF, Muen ke M. Holoprosen cephaly: recommendations for diagnosis and management. Curr Opin Pediatr. 2010;22(6):687-95.

11. 3.- OrioliIM, Castilla EE. Epidemiology of holoprosencephaly. Am J Med Genet C Semin Med Genet. 2010;154C:13-21.

12. 4.- Leoncini E, Baranello G, Orioli IM, Annerén G, Bakker M, Bianchi F, et al. Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surceillance systems: searching for population variations. Birth Defects Res A. 2008;82:585-91.

13. 5.- Orioli IM, Amar E, Bakker MK, Bermejo-Sánchez E, Bianchi F, Canfield MA, Clementi M, Correa A, Csáky- Szunyogh M, Feldkamp ML, Landau D, Leoncini E, Li Z, Lowry RB, Mastroiacovo P, Morgan M, Mutchinick OM, Rissmann A, Ritvanen A, Scarano G, Szabova E, Castilla EE. Cyclopia: an epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research. Am J Med Genet C Semin Med Genet. 2011;157C(4):344-57.

14. 6.- Sánchez J, Carstens E, Gutierrez J, Dezerga V, Sepúlveda W. Holoprocencefalia: Diagnóstico prenatal ultrasonográfico y manejo. Rev Chil Ultrasonog. 1998;1(4):120-23.

15. 7.- Saldarriaga W, Isaza C, Mastroiacovo P, Castilla EE. Cyclopia: a report of 4 cases born during a 170-day period in the Valle teaching hospital in Cali, Colombia. Rev Colomb Obstet Ginecol. 2007;58(1):70-7.

16. 8.- Poenaru MO, VilceaI D, Marin A. Holoprosencephaly:twocase reports. Maedica (Buchar). 2012;7(1):58-62.