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New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

MCHR2 gene duplications may be linked to alopecia areata.

Lower CD200R1 on certain immune cells is linked to more severe rheumatoid arthritis and immune imbalance.

CYLD deficiency in skin tumors disrupts hair follicle cell processes and protein secretion.

Four circRNAs were found to be significantly different in cashmere goat skin, affecting cashmere fineness.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

There's no significant link between the D19S884 marker at the insulin receptor gene and polycystic ovary syndrome.

PCOS in Karnataka is influenced by genetics, lifestyle, obesity, and diabetes.

More PDCD4 is linked to obesity, insulin problems, and cell death in ovaries for those with polycystic ovary syndrome.

A new mutation in the DCAF17 gene was found to cause Woodhouse-Sakati syndrome in a large family.

CD200 is not a reliable marker for identifying stem cells in all skin types.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Scientists developed a new way to study mutations in a skin condition using blood cells, which may help diagnose and treat the disease.

Targeting CD200 could be a new treatment for rheumatoid arthritis.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

Three characteristics of plasmacytoid dendritic cells help tell apart lupus-related hair loss from LPP.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Steroid treatment improved both gut and nerve symptoms in a man with Cronkhite–Canada syndrome.

The study concludes that mutations in the AEBP1 gene can cause a form of Ehlers-Danlos syndrome and should be considered in diagnosis.

cDermo-1 causes dense skin, feathers, and scales in chickens.

CCCA can appear as patchy hair loss in younger men, not just the usual pattern.

Fucoidan-derived carbon dots can effectively treat root canal infections by killing bacteria and are safer than traditional disinfectants.

Key circRNAs play a role in wool follicle development, aiding in breeding better quality wool sheep.

CCCA causes progressive hair loss in Black women, starting from a central scalp patch.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.

A genetic mutation in the DCAF17 gene caused Woodhouse-Sakati syndrome in a Chinese patient from a related family.

CCCA affects adolescents too, with genetic and environmental links, requiring careful diagnosis.

The wavy coat in NCT mice is caused by multiple genes, including a mutation in the Prss53 gene.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.