WAARDENBURG SYNDROME TYPE I IN AN IRANIAN FEMALE (A CASE REPORT)

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TAYEBI NAEIMEH

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Journal Paper

Paper Information

Journal: Iranian Journal of Pediatrics Year:2009 | Volume:19 | Issue:2 Page(s): 89-192

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Information Journal Paper

Title

WAARDENBURG SYNDROME TYPE I IN AN IRANIAN FEMALE (A CASE REPORT)

Author(s)

TAYEBI NAEIMEH | Issue Writer Certificate

Keywords

WAARDENBURG SYNDROME

WHITE FORELOCK

CONGENITAL SENSORINEURAL HEARING LOSS

Abstract

Background: WAARDENBURG SYNDROME (WS) is a rare, autosomal dominant disorder characterized by congenital hearing loss; dystopia canthorum; broad nasal root; depigmantation of hair, skin or both; and heterochromic iris. WS is classified into four types, WS1, WS2, WS3 and WS4. In this paper, we report a new case of WAARDENBURG SYNDROME type I in an Iranian female.Case presentation: This report describes a two-year-old female with WAARDENBURG SYNDROME type I with features such as unilateral profound sensorineural hearing loss, WHITE FORELOCK, dystopia canthorum, broad nasal root, hypopigmentation of skin and scalp defect.Conclusion: As no treatment is available for patients with WS1, conservative treatments such as skin graft and referral to a hearing specialist are crucial for the normal development of patients.

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APA: Copy

TAYEBI, NAEIMEH. (2009). WAARDENBURG SYNDROME TYPE I IN AN IRANIAN FEMALE (A CASE REPORT). IRANIAN JOURNAL OF PEDIATRICS, 19(2), 89-192. SID. https://sid.ir/paper/550685/en

Vancouver: Copy

TAYEBI NAEIMEH. WAARDENBURG SYNDROME TYPE I IN AN IRANIAN FEMALE (A CASE REPORT). IRANIAN JOURNAL OF PEDIATRICS[Internet]. 2009;19(2):89-192. Available from: https://sid.ir/paper/550685/en

IEEE: Copy

NAEIMEH TAYEBI, “WAARDENBURG SYNDROME TYPE I IN AN IRANIAN FEMALE (A CASE REPORT),” IRANIAN JOURNAL OF PEDIATRICS, vol. 19, no. 2, pp. 89–192, 2009, [Online]. Available: https://sid.ir/paper/550685/en

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