WOLF-HIRSCHHORN SYNDROME: REPORT OF TWO CASES IN BOSNIA AND HERZEGOVINA
Helji* S1,*, Hadzagic-Catibušic F1, Maksic H1, Terzic S1, Djozic M1, Mackic M2, Catovic A2
*Corresponding Author: *Corresponding Author: Dr. Suada Heljic, Pediatric Clinic, Clinical University Center Sarajevo, Bolnica 25, 71 000 Sarajevo, Bosnia and Herzegovina; Tel./Fax: +387-332-58481; E-mail: heljicsuada@hotmail.com
page: 77

REFERENCES

 1. Cooper H, Hirschhorn K. Apparent deletion of short arms of one chromosome (4 or 5) in a child with defects of midline fusion. Hum Chrom News 1961; 4:14-16.

2. Wolf U, Reinwein H. Porsch R, Schröter R, Baitsch H. Deficiency of the short arms of a chromosome No. 4. Humangenetik 1965; 1(5): 397-413.

3. Thies U, Back E, Wolf G, Schroeder-Kurth T, Hager HD, Scroder K. Clinical, cytogenetic and molecular investigations in three patients with Wolf- Hirschhorn syn drome. Clin Genet 1992; 42(4): 201-205.

4. Battaglia A, Carey JC, Cederholm P, Viskochil DH, Brothman AR, Galasso C. Natural history of Wolf-Hirsch horn Syndrome: experience with 15 cases. Pediatrics 1999; 103(4 Pt): 830-836.

5.OWJ. An epidemiological study of Wolf-Hirschhorn syndrome. Life expectancy and cause of mortality. J Med Genet 2001; 38(10): 674-679.

6. Ziška J. Diagnostica Syndromu a Malformaci. Praha: Galen. 1994; 245-246.

7. Matai S, Ganguly BB. Wolf- Hirschhorn (4p-) syn drome. Indian Pediatr 2003; 40(7): 681.

8. Sharathkumar A, Kirby M, Freedman M, Abdel haleem M, Chitayat D, Teshima IE, Dror Y. Malignant hematological disorders in children with Wolf- Hirschhorn syndrome. Am J Med Genet 2003; 119(2): 194-199.

9. Zollino M, Di Stefano C, Zampino G, Mastroiacovo P, Wright T, Sorge G, Selicorni A, Tenconi R, Zappala A, Battaglia A, Rocco M, Palka G, Pallota R, Altherr MR, Neri G. Genotype-phenotype correlations and clinical diagnostic criteria in Wolf-Horschhorn syndrome. Am J Med Genet 2000; 94(3):254-261.

10. Aslan H, Karaca N, Basaran S, Ermis H, Ceylan Y. Prenatal diagnosis of Wolf-Hirschhorn syndrome (4p-) in association with congenital hypospadias and foot defor mity. BMC Pregnancy Childbirth 2003; 3(1): 1.

11. Tachdian G, Fondacci C, Tapia S, Huten Y, Blot P, Nessman C. The Wolf-Hirschhorn syndrome in fetuses. Clin Genet 1991; 42(6): 281-287.

12. Quarrel OWJ, Snell RG, Curtis MA, Roberts SH, Harper PS, Shaw DJ. Paternal origin of the chromosomal deletion resulting in Wolf-Hirschhorn syndrome. J Med Genet 1991; 28(4): 256-259.

13. Wieczorek D, Krause M, Majewski F, Albrecht B, Horn D, Riess O, Gillessen-Kaesbach G. Effect of size of the deletion and clinical manifestation in Wolf-Hirschhorn syndrme: analysis of 13 patients with a de novo deletion. Eur J Hum Genet 2000; 8(7): 519-526.

14. Finzi S, Pinto CF, Wiggs JL. Molecular and clini cal characterization of a patient with a chromosome 4p deletion, Wolf-Hirschhorn syndrome, and congenital glau coma. Ophthalmic Genet 2001; 22(1):35-41.







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