Homocystinuria is an uncommon autosomal latent hereditary anomaly connected with essentially expanded degrees of homocysteine in the blood. The confusion is related with blood vessel and venous thromboembolic occasions at an early age. Patients may have a marfanoid habitus, mental hindrance, and mental issue. Skin appearances incorporate skin and hair hypopigmentation, a malar rash, livedo reticularis, and leg ulcers. Inadequacies of a few catalysts engaged with homocysteine digestion, including cystathionine β-synthase and 5,10-methylenetetrahydrofolate reductase, are related with homocystinuria.
Case Report: Journal of Vasculitis
Case Report: Journal of Vasculitis
Research Article: Journal of Vasculitis
Research Article: Journal of Vasculitis
Research Article: Journal of Vasculitis
Research Article: Journal of Vasculitis
Clinical image: Journal of Vasculitis
Clinical image: Journal of Vasculitis
Editorial: Journal of Vasculitis
Editorial: Journal of Vasculitis
Posters & Accepted Abstracts: Journal of AIDS & Clinical Research
Posters & Accepted Abstracts: Journal of AIDS & Clinical Research
Posters & Accepted Abstracts: Journal of AIDS & Clinical Research
Posters & Accepted Abstracts: Journal of AIDS & Clinical Research
Posters & Accepted Abstracts: Journal of AIDS & Clinical Research
Posters & Accepted Abstracts: Journal of AIDS & Clinical Research
Posters & Accepted Abstracts: Journal of Cosmetology & Trichology
Posters & Accepted Abstracts: Journal of Cosmetology & Trichology
Posters & Accepted Abstracts: Journal of Advanced Practices in Nursing
Posters & Accepted Abstracts: Journal of Advanced Practices in Nursing
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