Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Sonia Pramod Jain"'
Publikováno v:
Clinical Dermatology Review, Vol 6, Iss 1, Pp 55-55 (2022)
Xeroderma pigmentosum (XP) is an inherited condition with an extreme sensitivity to ultraviolet radiations. This condition mostly affects the eyes and areas of skin exposed to the sun and the nervous system. Here, we report a rare type XP E present i
Externí odkaz:
https://doaj.org/article/4b257180cd1e42b7afd94a511f1f5503
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 10, Iss 4, Pp WD01-WD02 (2016)
Netherton Syndrome (NS) is a rare autosomal recessive hereditary ichthyosiform disease with a classical triad comprising of an ichthyosiform dermatosis, hair shaft abnormalities and atopic diathesis. There is a mutation in a gene named Serine Protea
Externí odkaz:
https://doaj.org/article/94def50d52f04a41b88615eacc3c41c5
Autor:
Sonia Pramod Jain, Pramod Ajit Jain
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 7, Iss 4, Pp 744-745 (2013)
Adverse reactions to medications are extremely common and display a characteristic clinical morphology such as fixed drug eruption (FDE), Stevens-Johnson syndrome, urticaria, morbilliform exanthem, hypersensitivity syndrome, pigmentary changes, lic
Externí odkaz:
https://doaj.org/article/8242ac966b36416f81f9577ff05bb8cf