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The research showed that Vitamin D and its receptor are important for healthy bones and normal hair and skin in rats.

Eriocitrin and silymarin might be effective for hair loss treatment and need more research.

Gene therapy helped rats with a specific type of rickets grow hair without severe inflammation.

People with AB blood type may be more likely to get melasma.

A patient with Myotonic dystrophy type 1 had multiple tongue hemangiomas and was sensitive to anesthesia.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Green coffee bean extract didn't grow hair but reduced a hair loss-related enzyme in rats.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

Botulinum toxin type A helps treat hair loss by stopping cell death in hair follicles through a process involving certain non-coding RNAs and a protein called Bax.

Cationic and nonionic surfactants provide better color intensity and resistance for semi-permanent hair dye than anionic surfactants.

Laser treatment for hair loss works equally well on different skin types, but more research is needed for very dark skin.

A woman's hair grew back after treatment for a rare hair loss caused by proton therapy.

There is no cure for myotonic dystrophy type 1, so treatment focuses on managing symptoms and complications.

A 21-year-old male with a rare genetic disorder experienced sudden hair loss and high DHEAS levels, likely due to a condition similar to PCOS, usually seen in women.

Testosterone and dihydrotestosterone treatments can help with penile growth in males with 5α-reductase type 2 deficiency, with dihydrotestosterone being more effective in infancy.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Two siblings with a rare type of rickets and hair loss had low vitamin D levels, which is not typical for their condition.

Autoimmune Polyendocrine Syndromes involve specific combinations of autoimmune diseases.

KIF18B is important for correctly positioning cell division machinery in skin cells, affecting hair follicle development.

A man with a fungal scalp infection got better after treatment with griseofulvin, cetirizine, and ketoconazole shampoo.

Innate lymphoid cells type 1 may contribute to alopecia areata.

Innate lymphoid cells type 1 may contribute to alopecia areata by damaging hair follicles.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

Patients with one autoimmune disease should be checked for other autoimmune disorders.

WNT10B is linked to cancer development and affects survival and disease progression in various cancers.

Tailored nonsurgical cosmetic procedures are crucial for safely treating diverse skin types, especially skin of color.

Blocking 11β-HSD1 reduces stress hormone damage in hair growth cells.

A boy with Oculodentodigital syndrome had a unique GJA1 gene mutation causing his symptoms.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

Laminin-511 is involved in psoriasis development and can be regulated by cannabinoid receptor type 1.