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Mechanical trauma like towel drying can cause knotted hair even in straight hair.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

Lipase H is important for hair follicle function and shaping hair fibers.

Woolly hair is a rare genetic condition with no effective treatments.

Hair loss in certain mice is linked to changes in keratin-related genes.

CaBP1 and CaBP2 are important for continuous hearing by preventing inactivation of calcium currents in ear cells, with CaBP2 also able to restore hearing when reintroduced.

Mutations in the WNT10A gene cause Short Anagen Hair syndrome and increase the risk of male pattern hair loss.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Ageratum Conyzoides, when taken orally, can effectively reduce hair loss and improve hair growth.

Cosmetic products or emotional factors might contribute to Frontal Fibrosing Alopecia, and trichoscopy is useful for diagnosis.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Frontal Fibrosing Alopecia mainly affects postmenopausal Mexican women, requiring early detection to prevent permanent hair loss.

Certain gene variants can cause inherited hair diseases, which are important to diagnose and understand for patient care.

The study found that Frontal Fibrosing Alopecia in North-East India mainly affects middle-aged women and is often associated with lichen planus pigmentosus.

Most older adults experience pattern hair loss due to shrinking hair follicles, with men and women showing different balding patterns.

Hair examination helps diagnose rare neurological diseases in children.

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

An 8-year-old girl has a rare genetic disorder causing complete, irreversible hair loss and skin bumps.

Not having enough cystatin M/E protein causes less hair growth and dry skin.

Frontal fibrosing alopecia may be caused by an autoimmune reaction and hormonal imbalance.

The document concludes that a woman has both Frontal Fibrosing Alopecia and Lichen Simplex Chronicus, a previously unreported combination of conditions.

Thermal imaging is a useful non-invasive method to diagnose active inflammation in frontal fibrosing alopecia.

Treatment improved some symptoms but not all.

Researchers found a new area on chromosome 2 linked to a genetic hair loss condition.

Two siblings have a rare genetic condition causing curly, coarse hair.

Scalp reduction surgery is safe and effective for certain patients with hair loss, leading to dense hair coverage and high satisfaction.

Receding hairlines in men are uneven, with the right side larger than the left.

Topical minoxidil helps hair regrowth in over 50% of men and women.