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

CONCLUSIONS

 

Wolf-Hirschhorn syndrome (chromosome 4p deletion syndrome) presents a broad spectrum of possible pheno typic abnormalities, followed by developmental delay and mental retardation. Because of that, any case of IUGR associated with other anomalies (heart, skeleton, kidneys), requires prenatal chromosomal analysis. Postnatal recogni tion of WHS requires genetic testing of the parents and multidisciplinary supportive treatment.







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