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The meeting focused on understanding, diagnosing, and finding treatments for irreversible hair loss diseases.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

High levels of male hormones in pregnant mice cause heart enlargement and poor heart function in their female babies.

No link found between new male baldness genes and female hair loss.

The research suggests that autophagy-related genes might play a role in causing alopecia areata.

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

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

No link found between specific genes and female pattern hair loss.

The HOXC13 gene affects different hair proteins in cashmere goats in varied ways and is controlled by a feedback loop and other factors.

Certain gene mutations are linked to wool quality in sheep and could help in breeding for better wool.

Early hair loss links to metabolic issues in young Indian men.

Hormones and genes affect hair growth and male baldness.

People with X-linked hypohidrotic ectodermal dysplasia have no sweat ducts and less, thinner hair.

Obesity changes androgen levels in women with PCOS, leading to higher testosterone relative to androstenedione.

No link found between aromatase gene and female hair loss.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Researchers found two new genetic variants linked to Alzheimer's disease.

Certain gene variations are linked to higher male hormone levels in Chinese women with PCOS and insulin resistance.

Researchers found a new mutation in the EDA gene that likely causes missing teeth and mild skin symptoms in one family.

The mtDNA N haplogroup is linked to a higher risk of late-onset lupus and specific symptoms in Han Chinese women.

The conclusion suggests a new way to classify bradykinin-mediated angio-oedema based on different causes and its possible link with urticaria, which could improve diagnosis and treatment.

A gene deletion in mice causes weak protein, immune issues, hair loss, airway problems, and wasting disease.

The S250C variant in a gene may cause autoimmunity and immunodeficiency by impairing protein function.

Explosions don't stop hair proteins from being used to identify people.

Lack of cystatin M/E causes thin hair and dry skin.

The IRS-2 Asp/Asp genotype may increase the risk of PCOS in Chinese women, especially if they are not obese.

Certain gene variants in estrogen receptors are linked to polycystic ovary syndrome, mainly affecting metabolism, in Tunisian women.

HO-1 helps skin health and healing but can worsen melanoma; it's a potential treatment target for skin diseases.

MC4R gene variants not linked to female hair loss.