Autosomal recessive msmd due to partial ifngammar1 deficiency
An autosomal recessive condition caused by mutation(s) in the LDLRAP1 gene, encoding low density lipoprotein receptor adaptor protein 1. The phenotype is similar to that of familial hypercholesterolemia, but generally considered to be a milder form of hypercholesterolemia.
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A patient of 34 years complaining about having itching on the b/l palm region since 7-8 months and it has started from a small black patch . And it spreads in this condition. He has no history of DM and hypertension. N also No ho of smoking n alcohol.
Dr. Veenu Yadav4 Likes7 Answers - Login to View the image
Patient of Age 56 years came to the OPD with complaints of severe itching on the scalp since 2years and on plucking of hair he got some kind of relief.
Dr. Veenu Yadav1 Like6 Answers Pharma standards body Indian Pharmacopoeia Commission (IPC) has issued an alert over some commonly used medicines as they trigger adverse reactions. Commonly-used painkiller "Nimesulide" & antibiotic "Cefuroxime" can lead to serious skin disorders. In your practice and observation, have you noticed any such adverse reactions in patients in recent times?
Doc Insights0 Like5 Answers- Login to View the image
M37yrs. Pain neck referred to both hands. 6 months.
Dr. Syam Sundar Patro2 Likes4 Answers - Login to View the image
F.34yrs. Spot diagnosis please. No h/o Injury.
Dr. Syam Sundar Patro0 Like4 Answers