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Certain immune responses may cause ongoing COVID-19 symptoms like fatigue and brain fog.

Early diagnosis of PSIS can lead to normal height with growth hormone and testosterone treatment.

A pregnant woman with Werner's syndrome died during childbirth, but her baby survived and did not have the syndrome.

Coping style affects mental health and quality of life in Indian women with PCOS.

Sorafenib may cause hand-foot and stump syndrome, requiring early detection and management.

Hoyeraal-Hreidarsson syndrome in infants causes severe gastrointestinal issues.

Post-finasteride syndrome can cause lasting sexual, physical, and mental health issues with limited treatment options.

Shock wave therapy improved muscle function and movement in children with spastic cerebral palsy.

Stopping birth control pills may have triggered a manic episode in a woman with HAIR-AN syndrome.

A new mutation in the STING protein causes a range of symptoms and its severity may be affected by other genetic variations; treatment with a specific inhibitor showed improvement in one patient.

A teenage girl had both a rare ovarian tumor and a severe form of polycystic ovarian syndrome.

Some family members had a condition with both loose hair and unique eye changes, possibly indicating a new type of ectodermal dysplasia.

Early diagnosis and prednisone treatment can improve outcomes in Cronkhite-Canada syndrome.

A woman with Cushing's syndrome improved after surgery to remove an adrenal tumor.

A woman with ectopic Cushing's syndrome and COVID-19 passed away despite treatment.

Vogt-Koyanagi syndrome often leads to partial or complete blindness and responds poorly to treatment.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Topoisomerase inhibitors can cause hair loss, skin rash, hand-foot syndrome, and nail changes.

The patient has a leg condition caused by vein issues, needing lifestyle changes and leg care.

Mutations in the KLHL24 gene cause a skin disorder in some Russian families.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

CMG2 and TEM8 receptors have distinct roles in skin and growth disorders, affecting collagen breakdown and growth.

Controlling Tslp can improve health in AEC syndrome patients.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

A woman's rare scalp condition worsened after using a specific arthritis medication, suggesting such medications can sometimes trigger or aggravate psoriasis.

Scientists used stem cells to create a model of the skin disease Epidermolysis Bullosa simplex, which helped them understand its molecular mechanisms and could aid in finding treatments.

Many dermatology patients experienced anxiety, depression, PTSD, and skin issues after the February 6, 2023 earthquakes, highlighting the need for combined skin and mental health care.

SLE significantly affects daily life, especially through fatigue and joint pain, highlighting the need for better treatments.

The report described a unique case of Cronkhite-Canada syndrome with unusual polyps and an association with multiple myeloma.

Hidradenitis suppurativa may be more severe in people with Mediterranean fever gene mutations.