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A possible link exists between minimal change nephrotic syndrome and complete hair loss.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

Abnormal T-cells from thymomas cause non-motor symptoms in some myasthenia gravis patients.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Renal histology is crucial for diagnosing simultaneous SLE and IgG4RD.

Lower levels of MYLK and CALD1 in bladder cancer and osteosarcoma are linked to worse survival rates.

Folliculotropic mycosis fungoides has unique molecular features and cell interactions that could guide targeted therapy.

Certain proteins involved in DNA modification may affect the genetic changes in systemic lupus erythematosus and could indicate the disease's activity.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Mycosis fungoides can have unusual symptoms and may be misdiagnosed, but specific cell markers might suggest a lower risk of worsening.

Autoimmune polyglandular syndrome can cause temporary brain issues that may improve on their own.

Mogamulizumab can cause hair loss, often linked to a better treatment response.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

Benign follicular mucinosis involves immune cells attacking hair follicles.

A woman's hair loss, resembling an autoimmune condition, improved after treatment, but requires ongoing checks due to potential serious associations.

Pemphigus vulgaris involves specific immune cells and B cells that produce antibodies causing skin blisters.

An 8-year-old girl developed a rare skin condition in a linear pattern on one side of her body after a lung infection, which improved with treatment.

Personalized sonidegib dosing can effectively treat Gorlin-Goltz syndrome with fewer side effects.

A young woman with a rare skin cancer was diagnosed late because her symptoms were unusual for the disease.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

Most patients experienced mild to moderate skin problems during a trial for a desmoid tumor treatment.

Dermal IgA deposition without symptoms is rare in Dermatitis herpetiformis risk groups.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

The term "low-risk" in myelodysplastic syndrome is misleading and should be changed to better reflect patient experiences and needs.

A scalp biopsy revealed systemic amyloidosis in a woman who initially seemed to have a common hair loss condition.

A woman was wrongly diagnosed with lupus but actually had leprosy.

A man with a type of skin lymphoma had unusual yellowish skin growths despite normal blood lipid levels, and treatment reduced some symptoms but not the growths.

Some skin growths with mucin can form hair follicles and resemble skin cancer, but a special stain can help tell them apart.

Early and accurate diagnosis of congenital smooth muscle hamartomas is crucial to distinguish them from other conditions.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.