Ocular Findings of Incontinentia Pigmenti in a Male Infant With Klinefelter Syndrome

1992 ◽  
Vol 29 (3) ◽  
pp. 180-184
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Susan M Fowell ◽  
Mark J Greenwald ◽  
Julie S Prendiville ◽  
Lee M Jampol
1989 ◽  
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Skaidra Valiukeviciene

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...  

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Vol 32 (1) ◽  
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Mariya Moosajee ◽  
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Sui Chien Wong

1970 ◽  
Vol 10 (1) ◽  
pp. 25-27
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Md Wahiduzzaman

Incontinentia pigmenti (IP) is an uncommon disorder which can affect the skin and other systems. . It is an X-linked dominant genodermatosis mainly affecting the female baby with prenatal lethality in boys. It was first reported by Garrod in 1906 and further defined by Bloch and Sulzberger in 1926 and 1928. It can involve the skin only or in addition can affect the central nervous system, eyes and the teeth. The boys do not survive unless associated with Klinefelter syndrome (47, XXY). Morbidity and mortality are related to neurologic and ophthalmologic sequelae. Our presented case did not have any systemic involvement but only cutaneous symptoms. doi:10.3329/jom.v10i1.2000 J Medicine 2009; 10: 25-27


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