Arthropathic_psoriasis= اعتلال المفاصل الصدفي

Arthropathic_psoriasis= اعتلال المفاصل الصدفي Arthropathic psoriasis     Psoriatic arthritis is a form of arthritic joint disease associated with the chronic skin scaling and fingernail changes seen in psoriasis. Description Physicians recognize a number of different forms of psoriatic arthritis. In some patients, the arthritic symptoms will affect the small joints at the ends of […]

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Ashy dermatosis= الجلاد الرمادي

Ashy dermatosis= الجلاد الرمادي Ashy dermatosis   Ashy dermatosis is a controversial entity that has received many names in the literature. It has sometimes been associated with other diseases, and sometimes considered a variant of lichen planus (LP) .   Some authors suggest that the condition is no more than a post-inflammatory pigmentary change in […]

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Aspergillosis= داء الفطور الرشاشية

Aspergillosis= داء الفطور الرشاشية Aspergillus species are ubiquitous molds found in organic matter. Although more than 100 species have been identified, the majority of human illness is caused by Aspergillus fumigatus and Aspergillus niger and, less frequently, by Aspergillus flavus and Aspergillus clavatus. The transmission of fungal spores to the human host is via inhalation. Also see the eMedicine articles Aspergillosis (dermatology focus), Aspergillosis (pediatric […]

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Ataxia-telangiectasia= الهزع المخيخي مع توسع الشعريات

Ataxia-telangiectasia= الهزع المخيخي مع توسع الشعريات EPIDEMIOLOGY   Ataxia-telangiectasia , also called Louis-Bar syndrome, is an autosomal recessive disorder with an incidence of approximately 1:40,000 and a carrier rate of up to 1 percent. Carriers have an increased risk of breast cancer, hematologic malignancies, and ischemic heart disease, with a reduced life expectancy of approximately 8 years.111 These heterozygotes show increased risk of […]

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Atrichia Congenita Circumscripta =المَرَط الخلقي المتحدد

Atrichia Congenita Circumscripta =المَرَط الخلقي المتحدد Abstract Congenital atrichia is a rare autosomal recessive disorder of hair development, characterized by complete loss of hair shortly after birth. Evidence of linkage to chro­mosome 8p12 has been established, implicating the human homolog of the mouse hairless (hr) gene as a candidate gene. We have previously identified missense mutations […]

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