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Androgenic alopecia is a type of hair loss that's partly inherited and can be due to hormonal imbalance.

A rare genetic disease causes rickets and often hair loss in young children, which can improve with specific treatments.

Pregnant women with Systemic Lupus Erythematosus have a higher risk of blood clotting problems.

Monilethrix is a rare, inherited condition causing fragile hair and hair loss, with no cure but some treatments may help.

Epidermolysis bullosa is a genetic disease causing fragile skin and blisters in both animals and humans.

Cronkhite-Canada syndrome may be more treatable and less severe than previously thought.

Darier-White disease causes skin and nail issues, starts around age 20, worsens until 40-50, and has poor treatment options.

Caffeine in Alpecin shampoo may help prolong hair root activity and reduce hair loss.

AGA causes hair loss by shrinking hair follicles due to DHT binding, and can be treated with finasteride and minoxidil.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Myoblast transplantation shows promise for treating various muscle and heart conditions.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Genetic mutations cause various hair diseases, and whole genome sequencing may reveal more about these conditions.

A boy with a rare skin condition improved quickly after starting zinc supplements.

Hair loss treated with minoxidil, finasteride, laser/light, hair transplant, and scalp prostheses; more research needed for skin of color.

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Self-amplifying RNA could be a better option for protein replacement therapy with lower doses and lasting effects, but delivering it into cells is still challenging.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

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

Pattern hair loss is mainly caused by genetics and hormones, with limited effective treatments available.

A man with myotonic dystrophy type 1 had 28 skin cancers, suggesting a link between the disease and skin cancer, emphasizing the need for sun protection and regular skin checks.

The study concluded that key signs of Keratosis follicularis spinulosa decalvans are changes in terminal hair and vellus hair follicles, which likely start the inflammation and damage to hair follicles.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Some people with alopecia areata, a hair loss condition, get better within a year without treatment, but it can happen again.

Female pattern hair loss is common, often starts in the 30s or 40s, worsens after menopause, and can negatively affect quality of life.

Hirsutism is often caused by high male hormone levels and can be treated with lifestyle changes and medications.

A new food supplement was highly effective in curing hair loss in young men.