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El-Kamah GY et al. - Infantile systemic hyalinosis (ISH) (MIM 236490) is a rare, progressive, fatal autosomal recessive condition characterized by widespread deposition of hyaline material in many tissues. The authors proband was a 4-year-old male with growth retardation, severe labio-gingival enlargement, generalized stiff skin, joint contractures, and intractable diarrhea.

Today in Basic Science/Genetics...keeping you current

Skin pigmentation after NB-UVB and three analogues of prostaglandin F2
Journal of the European Academy of Dermatology and Venereology, 12/16/09

Expression of Ca2+-Activated K+ Channels in Human Dermal Fibroblasts and Their Roles in Apoptosis
Skin Pharmacology and Applied Skin Physiology, 12/16/09

Beclin 1 and LC3 autophagic gene expression in cutaneous melanocytic lesions
Human Pathology, 12/16/09