عنوان
پدید آورنده
موضوع
رده
کتابخانه
محل استقرار
NATIONAL BIBLIOGRAPHY NUMBER
Number
LA72c3461z
LANGUAGE OF THE ITEM
.Language of Text, Soundtrack etc
انگلیسی
TITLE AND STATEMENT OF RESPONSIBILITY
Title Proper
Lipoid Proteinosis: a case report in two siblings
General Material Designation
[Article]
First Statement of Responsibility
Ranjan, Rashmi; goel, khushbu; sarkar, rashmi; garg, vijay kumar
SUMMARY OR ABSTRACT
Text of Note
Lipoid proteinosis was first reported by Urbach and Wiethe in 1929. It is also known as hyalinosis cutis et mucosae or Urbach-Wiethe disease. It is a rare autosomal recessive disorder and characterized by the infiltration of hyaline material in the skin, oral cavity, larynx, and internal organs. Lipid proteinosis presents early in life. Hoarseness develops in infancy. The classic sign is beaded eyelid papules along the lid margin, also known as 'Monilform Blepherosis'. In India about 30 cases have been reported to date. We report the following case because of its rarity in the Indian literature.
SET
Date of Publication
2015
Title
Dermatology Online Journal
Volume Number
21/3
PERSONAL NAME - PRIMARY RESPONSIBILITY
Entry Element
Ranjan, Rashmi; goel, khushbu; sarkar, rashmi; garg, vijay kumar
ELECTRONIC LOCATION AND ACCESS
Electronic name
مطالعه متن کتاب [Article]
275578
a
Y
