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Paper Information

Journal:   IRANIAN JOURNAL OF DERMATOLOGY   Summer 2003 , Volume 6 , Number 4 (24); Page(s) 51 To 54.
 
Paper: 

LEOPARD SYNDROME: REPORT OF A CASE

 
 
Author(s):  RAMAZANPOUR A.*, BABAEI HOSSEIN
 
* Department of Dermatology, Zanjan University of Medical Sciences, Zanjan, Iran
 
Abstract: 

LEOPARD syndrome is an autosomal dominant hereditary disease, which is characterized with cutaneous pigmented patches, electrocardiographic changes, ocular hypertelorism, retarded growth, pulmonic stenosis, genital abnormalities and congenital deafness. The gene of this disease has high penetrance but expression is varied and incomplete forms may be seen. We report a 23 year-old woman with mucocutaneous pigmented patches, congenital deafness, delayed puberty and ECG changes. It seems that this case is an incomplete form of LEOPARD syndrome.

 

 

 

 
Keyword(s): LEOPARD SYNDROME, INCOMPLETE FORMS, PIGMENTED PATCH, CONGENITAL DEAFNESS
 
 
References: 
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Citations: 
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+ Click to Cite.
APA: Copy

RAMAZANPOUR, A., & BABAEI, H. (2003). LEOPARD SYNDROME: REPORT OF A CASE. IRANIAN JOURNAL OF DERMATOLOGY, 6(4 (24)), 51-54. https://www.sid.ir/en/journal/ViewPaper.aspx?id=48100



Vancouver: Copy

RAMAZANPOUR A., BABAEI HOSSEIN. LEOPARD SYNDROME: REPORT OF A CASE. IRANIAN JOURNAL OF DERMATOLOGY. 2003 [cited 2021October21];6(4 (24)):51-54. Available from: https://www.sid.ir/en/journal/ViewPaper.aspx?id=48100



IEEE: Copy

RAMAZANPOUR, A., BABAEI, H., 2003. LEOPARD SYNDROME: REPORT OF A CASE. IRANIAN JOURNAL OF DERMATOLOGY, [online] 6(4 (24)), pp.51-54. Available: https://www.sid.ir/en/journal/ViewPaper.aspx?id=48100.



 
 
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