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Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

Lipedema is a painful fat disorder in women that's hard to treat, often worsens with hormonal changes, and requires symptom-focused therapies.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

Two drugs, finasteride and minoxidil, are approved for hair loss treatment, but new therapies are being developed.

A one-year-old cat had multiple benign skin tumors similar to those known in humans.

A baby had a rare case of widespread milia, which was treated and is being monitored.

A condition called Central Centrifugal Cicatricial Alopecia causes hair loss and scalp burning in middle-aged African women, and it's treated with various medications, hair transplants, and non-drug methods like wigs.

Nilotinib can cause generalized keratosis pilaris.

Ashwagandha may improve hormone levels and reduce hair loss in non-classical adrenal hyperplasia.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

Androgenetic alopecia, or hair loss, is caused by a mix of genetics, hormones, and environment, where testosterone affects hair growth and causes hair to become smaller and grow for a shorter time.

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Hidradenitis suppurativa might be a type of autoinflammatory skin disease.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

A specific gene variant is linked to a higher risk of hair loss from chemotherapy in breast cancer patients.

The conclusion is that genetic testing is important for diagnosing and treating various genetic hair disorders.

Bioengineering can potentially treat hair loss by regenerating hair follicles and cloning hair, but the process is complex and needs more research.

TGM3 is important for skin and hair structure and may help diagnose cancer.

Low levels of vitamin B12 and ferritin are linked to early hair graying.

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

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.

A condition with certain scalp changes may come before acne keloidalis nuchae and other similar hair loss disorders.

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.

Certain genetic markers linked to wool quality in Rambouillet sheep were identified, which can guide better breeding choices.