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Anti-epileptic drugs may cause visual and hair side effects due to enzyme inhibition, especially in genetically predisposed individuals.

Upadacitinib improved both Crohn's ileitis and alopecia universalis in a patient.

The patient's hair improved after treatment, but the genetic link is unclear.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

Traditional Chinese medicine may help relieve symptoms of Cronkhite-Canada syndrome.

Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

Gene sequencing is essential for diagnosing junctional epidermolysis bullosa.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

A patient had both chronic lupus and systemic scleroderma, requiring careful treatment to manage symptoms.

A girl with Turner syndrome had psoriasis, alopecia areata, and trachyonychia.

The young woman has a benign, hereditary skin condition with no signs of a more serious syndrome.

A woman's cyclic Cushing syndrome was caused by a tumor in her adrenal gland that produced ACTH.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

A patient with a nerve disorder died from infection complications after developing insulin resistance from a treatment.

Severe hair loss (androgenetic alopecia) is linked to higher risk of heart disease (cardiovascular atherosclerosis).

Minimally invasive glaucoma surgery can effectively manage glaucoma in GAPO syndrome when other treatments fail.

Alopecia areata may increase the risk of cardiovascular disease.

Frontal fibrosing alopecia might be linked to autoimmune diseases.

SAHA syndrome links oily skin, acne, excess hair, and hair loss in women, similar to PCOS.

The boy likely has a fungal infection causing hair loss.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

A complex X chromosome rearrangement can increase the risk of multiple autoimmune diseases.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

Adding colchicine stopped the girl's recurring heart issues caused by lupus.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Rhupus is a complex syndrome that combines rheumatoid arthritis and lupus, making diagnosis challenging.

The A allele of the C2 gene increases the risk of lupus, while the G allele may protect against it.

Correct diagnosis and treatment of lupus vasculitis improved the woman's severe symptoms.

A 16-year-old boy with lupus had a rare brain artery issue but fully recovered with treatment.