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Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

A woman was diagnosed with porphyria cutanea tarda and improved with phlebotomy and lifestyle changes.

Hair analysis can't determine ponies' calcium and phosphorus levels; use soil and feed tests instead.

Pregnancy can cause various skin changes and diseases, with PUPPP being the most common skin condition specific to pregnancy.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

A dog developed skin issues from too many steroids, but reducing steroids and using a specific treatment fixed the problems.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

The document concludes that accurate diagnosis and appropriate management are crucial for treating various hair disorders, which have significant psychological impacts.

Genetic screening is crucial for accurately diagnosing APS-1 due to its varied symptoms.

Skin changes can help diagnose and manage endocrine disorders like thyroid problems, diabetes, and adrenal gland conditions.

Most skin changes during pregnancy are harmless and temporary, but some can risk the fetus and need careful treatment.

Most pregnant women experience skin changes like darkening and itching, while serious skin conditions are rare but need early treatment.

High prolactin levels might be linked to hair loss in autoimmune thyroid disease, but more research is needed.

An 11-year-old child with total hair loss may have a genetic autoimmune disease, and the outlook for hair regrowth is not good.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Half of people with Alopecia Areata may see hair regrowth within a year without treatment, but recovery is unpredictable.

Thymus transplantation successfully restored immune function in infants with FOXN1 deficiency.

New treatments for Alopecia Areata show promise but need to be more effective and affordable.

Alopecia Areata is an autoimmune condition often starting before age 20, with varied treatment success and a need for personalized treatment plans.

People with diabetes or obesity should manage their conditions carefully as they have a higher risk of severe COVID-19.

Some drugs can cause hair loss, and stopping these drugs often leads to hair regrowth.

Azathioprine's effectiveness and safety require careful monitoring and more research, especially regarding its use with corticosteroids and the role of TPMT status in patients.

Adrenal disorders can cause lasting brain and behavior issues in children.

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

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

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

The cause of alopecia areata was unknown, and while various treatments existed, no best treatment was agreed upon.

A young man with an eating disorder had a life-threatening adrenal crisis due to an autoimmune condition, highlighting the need for better education on managing hormone treatments.