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Using SNP array testing helped quickly find the gene causing Woodhouse-Sakati syndrome in two related individuals.

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

Friedreich's ataxia causes thin, weak hair with surface damage and cavities.

Gene therapy has potential as a future treatment for Hutchinson-Gilford progeria syndrome.

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

CG2001 is safe and well-tolerated for treating hair loss, with fewer side effects than oral finasteride.

Myotonic Dystrophy may age cells faster, and drugs that target aging could be potential treatments.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

A new fluorescent material can detect dextran sulfate sodium, turning green when present, useful for forensic and environmental monitoring.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

A new gene mutation causes vitamin D resistance and hair loss in two unrelated girls.

A mycobacterial protein shares a similar region with a human skin protein, possibly affecting skin diseases.

New genetic mutations linked to rare skin disorders were found in three newborns.

A new mutation in the FLCN gene linked to Birt-Hogg-Dube syndrome was found, suggesting people with certain lung collapse should be tested for this mutation and screened for kidney and colon cancer.

TAK-279 effectively reduces psoriasis symptoms and is safe.

γδTregs may help treat autoimmune diseases like alopecia areata by promoting hair regrowth and reducing immune attacks.

Finger length ratio may indicate male hair loss.

Small molecules can help turn skin cells into sweat gland-like cells for potential skin repair.

The hydrogel helps heal wounds and regrow hair by mimicking a baby's environment.

LncRNA018392 helps goat skin cells grow by increasing CSF1R.

A specific DNA pattern in Malassezia restricta may be linked to hair loss in men.

A chromosomal change may cause ectodermal dysplasia and developmental issues in a child.

CG2001 is safe, well-tolerated, and a promising treatment for hair loss with fewer side effects.

Live vaccines can be safely given to infants with a FOXN1 variant if their immune function improves over time.

Umbilical cord blood transplantation improved the boy's symptoms despite complications.

A gene called Gk5 controls lipid production in the skin and affects hair growth.