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

Androgens can both increase body hair and cause scalp hair loss.

Acne is a chronic skin condition not caused by poor hygiene or diet, and it requires long-term treatment and patient education.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Different hair and scalp disorders cause hair loss or excess hair growth, with various treatments available depending on the specific condition.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.

Current treatments for common male hair loss have limited effectiveness and can cause side effects.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

The research found that male pattern hair loss is mostly genetic and involves hair thinning due to hormonal effects and changes in gene expression.

Mutations in the glucocorticoid receptor gene cause reduced sensitivity to glucocorticoids and may lead to poor response to treatment.

Certain genes are linked to type 1 and type 2 diabetes in kids, and changes in these genes can also cause other diabetes-related conditions.

Removing a specific gene in certain skin cells causes hair loss on the body by disrupting normal hair development.

Netherton Syndrome is a non-treatable genetic disorder in children causing skin, hair, and allergy issues.

Polycystic Ovary Syndrome (PCOS) is a common condition in women that can cause metabolic, reproductive, and psychological issues, and requires lifestyle changes and medication for management.

Polycystic Ovary Syndrome likely starts in childhood and may be genetic and influenced by early hormone exposure.

The study concluded that immune cells attacking hair follicles cause hair loss in alopecia, with genetics and environment also playing a role, and highlighted the potential of certain treatments.

Low-dose radiation affects hair stem cell function and survival by changing their genetic material's structure.

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

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

Polycystic Ovary Syndrome (PCOS) is a hormonal disorder in women that can cause infertility and other health issues, and it may be improved by treatments that increase insulin sensitivity.

Melanocytes produce melanin; their defects cause vitiligo and hair graying, with treatments available for vitiligo.

Hair loss can be treated based on its type and cause, improving quality of life.

Multi-omics techniques help understand the molecular causes of androgenetic alopecia.

Hair loss without scarring is more common than permanent hair loss with scarring, and is often due to genetic factors.

Minoxidil improved hair growth in a child with a rare genetic disorder.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Despite progress in treatment, the exact cause of Alopecia areata is still unknown.

The document concludes that better treatments for CCCA are needed and more research is required to understand its causes related to hairstyling and genetics.