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FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

The document concludes that eyelash trichomegaly, which is the abnormal growth of eyelashes, can be present from birth, caused by diseases, or result from certain medications.

The FOXN1 gene is crucial for developing immune cells and preventing immune disorders.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

Tacrolimus is an effective treatment for several skin conditions with fewer side effects than cyclosporine.

The document is a detailed medical reference on skin and genetic disorders.

Skin symptoms can indicate endocrine disorders and have various treatments.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

Alopecia areata is an autoimmune disease where T cells attack hair follicles.

Wharton's jelly-derived stem cells were safely used to treat four alopecia patients, resulting in hair regrowth in all of them.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

JAK inhibitors show promise for treating hair loss in alopecia areata but need more clinical trials to confirm safety and effectiveness.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Different causes of beard hair loss have various treatments, including medications, lifestyle changes, and procedures to stimulate hair growth.

Hair loss from Alopecia Areata is caused by both genes and environment, with several treatments available but challenges in cost and relapse remain.

MSC exosome therapy improved hair quality in patients with acquired trichorrhexis nodosa.

Alopecia in patients with epidermolysis bullosa varies in severity and is often caused by skin blistering or trauma.

PRP is effective for treating hair loss, improving hair density, count, and thickness.

The report concludes that PCOS is mainly a condition of excess male hormones and its definition may change as new information is discovered.

JAK inhibitors show promise for treating skin conditions like eczema, hair loss, and psoriasis.

JAK inhibitors can effectively reverse hair loss in people with alopecia areata.

The document concludes that Telogen Effluvium is a hair loss disorder that can be assessed with the modified wash test and may be treated with clobetasol foam, with patient management being important.

Changes in the SREBF1 gene cause a rare genetic skin and hair disorder.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Thyroid diseases may contribute to autoimmune skin diseases, and more research is needed on their relationship.

The document concludes that changes in eyelashes and eyelid skin can indicate various local and systemic diseases.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.