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The study concluded that patients with total hair loss and recurring hair loss had an earlier onset, longer-lasting condition, and a greater negative impact on their quality of life, with allergic conditions linked to more severe hair loss.

Babies born after 38 weeks to mothers under 36 years old and not delivered by C-section have a higher risk of neonatal occipital alopecia.

Hair loss can be treated with medications like minoxidil and finasteride or surgery, but treatment effectiveness varies by alopecia type and accurate diagnosis is important.

Finasteride solution helps treat hair loss.

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

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

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

Hair loss in children is often caused by scalp infections, immune disorders, hair pulling, stress, and requires careful treatment due to emotional effects.

A girl with lupus had unusually long and thick eyelashes, a rare symptom of her condition.

miR-199a-3p controls hair growth and is linked to alopecia areata.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

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

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

An 11-year-old girl with Trichotillomania developed a large hairball in her stomach, treated with medication, therapy, and family education.

An 11-year-old girl with a hair-pulling disorder had a hairball in her stomach and was treated with medication, therapy, and a team of doctors.

Alopecia areata is a genetic and immune-related hair loss condition that is often associated with other autoimmune diseases and does not typically cause permanent damage to hair follicles.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

The guide helps dermatologists diagnose and treat different types of hair loss.

A patient developed nerve problems as a side effect of a hair loss treatment called tofacitinib.

Hypothyroidism may cause certain types of hair loss.

A rare bacterial infection of pubic hair can cause strong genital odor, but trimming hair and using clindamycin can quickly fix it.

Using animal names for skin conditions helps with learning and memory.

A child with a rare vitamin D-resistant condition improved with treatment.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

A girl with a rare genetic condition affecting hair and nails also developed a common type of hair loss, suggesting a possible genetic link.

Oral minoxidil and growth factors improved hair density and thickness in a girl with hereditary hair loss.

A mix of methotrexate, corticosteroids, and topical minoxidil effectively treated severe total body hair loss, but caused stretch marks and needs long-term monitoring.

Trichotillomania involves hair pulling and can be treated with therapy and medication.

People with the same genetic mutation for Woodhouse-Sakati syndrome can have different symptoms.

Trichotillomania in dementia may be better treated with dopamine blockers like quetiapine than with SSRIs.