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CASE REPORT
Year : 2019  |  Volume : 10  |  Issue : 2  |  Page : 158-161

Barber Say Syndrome (A new case report)


1 Department of Neonatology, Neonatology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran
2 Department of Pediatrics, Shiraz University of Medical Sciences, Shiraz, Iran
3 Department of Family Medicine, Shiraz University of Medical Sciences, Shiraz, Iran

Correspondence Address:
Hourvash Haghighinejad
Department of Family Medicine, Shiraz University of Medical Sciences, Shiraz
Iran
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/idoj.IDOJ_68_18

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Barber Say syndrome (BSS) is a rare ectodermal dysplasia with neonatal onset characterized by congenital generalized hypertrichosis, atrophic skin, ectropion and macrostomia. A literature review showed less than 20 previously reported cases of Barber Say syndrome. This presentation reports a one day old female with syndrome face, low hairline, coarse face, macrostomia, thin upper lip, bilateral ectropion and hypertelorism, hypertrichosis, senile skin appearance, hypoplastic nipples and one area of mild skin atrophy. These findings are consistent with BSS.


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