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Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

If someone has scaly skin, muscle stiffness, and intellectual disability, doctors should consider Sjogren-Larsson Syndrome, but other conditions if more symptoms are present.

Researchers found a new ABCD1 gene mutation linked to a rare brain and nerve disorder with unusual brain changes.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

The unique coat of lykoi cats is likely caused by new variants in the Hairless gene.

Finasteride nano-emulsion optimized using chemometric approach.

A man with X-ALD improved after treatment, highlighting the need to consider X-ALD in similar patients and test their relatives.

Finasteride, a hair loss treatment, works better and is more stable when delivered through specially prepared gels, leading to increased hair growth.

A new type of hereditary hair loss in a Chinese family is linked to chromosome 2p25.1–2p23.2.

The new finasteride delivery system using chitosan-based nanoniosomes shows promise for prostate cancer prevention.

The dutasteride nanoemulsion could improve hair loss treatment by enhancing drug penetration and retention in hair follicles.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

The procedure is effective for reducing the forehead despite potential for visible scars.

The gel effectively delivers dutasteride for hair loss treatment and remains stable for 90 days.

Scientists are using clumps of special stem cells to improve organ repair.

A new syndrome was linked to two new genetic changes in the MBTPS1 gene in a 14-year-old girl.

Platelet-rich gel is an effective treatment for healing scalp wounds with exposed skull.

The article concludes that creating a detailed map of normal human skin at the single-cell level is important.

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

The F2 Emulgel with Tridax procumbens extract showed good physical properties and antimicrobial effectiveness for wound healing.

The F2 Emulgel with Tridax procumbens extract showed the best qualities for healing wounds.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

ROP GTPase helps control the growth of pollen tubes and root hairs by managing cell structure and movement.

Hair examination helps diagnose rare neurological diseases in children.

A Chinese male with a new genetic mutation has a skin condition and severe urinary issues, with treatments having mixed success.

A boy with a rare skin condition improved quickly after starting zinc supplements.

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

A mother and daughter have a rare genetic hair loss disorder with no effective treatment.