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Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

Biotin supplements significantly improved a young girl's uncombable hair.

A girl with skin rashes and low zinc levels improved with zinc supplements and had new gene mutations linked to her condition.

Congenital Adrenal Hyperplasia is a rare inherited disease causing hormone imbalances, affecting growth, fertility, and heart health, diagnosed through blood tests and treated with medication and lifestyle changes.

Hair color is determined by melanin and can be affected by genetic conditions like albinism.

Foals can have various skin issues, some genetic, immune-related, or due to infections and allergies.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

A gene mutation in Lama3 is linked to a common type of hair loss.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Cantú syndrome is caused by mutations in the ABCC9 gene.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

A specific gene mutation causes congenital hair loss.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

The fuzzy gene is crucial for controlling hair growth cycles.

The document talks about hard-to-treat and rare acne types, their connection with other health issues, the importance of correct diagnosis, and the challenges in managing them.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

The genes KRT25 and SP6 affect curly hair in horses, with KRT25 also causing hair loss. If both genes are mutated, the horse gets curly hair and hair loss. KRT25 can hide the effect of SP6.

A 4-year-old boy with a rare type of rickets and hair loss improved in bone health but not hair growth after vitamin D and calcium treatment.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

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

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Laser hair removal is effective for hirsutism when combined with treatment for the underlying causes.

Sudden, unusual hair loss may indicate serious underlying health issues.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

"D-CHRAMPS syndrome" is a newly identified condition with multiple severe symptoms.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.