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The conclusion is that cerebrovascular diseases can cause seizure-like activity in stroke patients, which can be improved with antiepileptic drugs.

A woman with both Cronkhite-Canada syndrome and myelodysplastic syndrome improved significantly with corticosteroid treatment.

The case shows how hard it is to tell apart Multiple Autoimmune Syndrome from other similar autoimmune conditions, but correct diagnosis is key for treatment to work.

The rs231775 genetic variant is linked to a higher risk and severity of Alopecia Areata in males.

Systemic lupus erythematosus is an autoimmune disease causing diverse symptoms and major organ involvement.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

CCCA and LPP may be related hair loss conditions influenced by genetics and environment, needing early treatment.

Hair root analysis can effectively detect somatic mosaicism in double cortex syndrome.

Chronic granulomatous disease may be linked to developing systemic lupus erythematosus.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

Mutations in the PADI3 gene may cause central centrifugal cicatricial alopecia in women of African ancestry.

CCCA is a scarring hair loss condition mainly in African descent women, possibly caused by genetics and hairstyling, treated with gentle hair care and medications.

Certain genetic variants in ERN1, TACR3, and SPPL2C are linked to when Alzheimer's disease starts.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

The report found a new type of hair loss in African-American women that affects more areas of the scalp than previously thought.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

CCCA affects adolescents too, with genetic and environmental links, requiring careful diagnosis.

Alopecia areata patients have a higher risk of subclinical atherosclerosis, and carotid ultrasound can help assess their cardiovascular risk.

The conclusion is that hair loss from CCCA may be genetic and not solely caused by hair grooming practices.

A young man developed a rare, bilateral scalp condition after head trauma, causing hair loss but no neurological or eye issues.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Blocking the CCR5 receptor may be a new way to treat hair loss from alopecia areata.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

Certain genes are linked to the risk of developing Alopecia Areata.

Men with Addison disease should be screened for X-linked adrenoleukodystrophy if they have hair loss.

A patient with a rare disease had a unique genetic mutation linked to their symptoms.

Severe CCCA may be biologically and clinically different from milder forms.

Early recognition and a multidisciplinary approach are crucial for effectively managing complex autoimmune conditions like SLE with CAPS and AHA.

MRI can show unusual brain changes in adrenomyeloneuropathy.