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A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Recent hair loss research shows some progress, especially in understanding male pattern baldness, but effective treatments for many types of hair loss are still lacking.

Up to 50% of scalp hair can be lost before it appears thin, and treatment is only needed for hair loss caused by diseases or deficiencies.

Scientists found gene mutations that affect hair loss, skin stem cells, and skin disorders, and identified drugs that may help treat blood vessel and skin conditions.

Genetic mutations can cause hair growth disorders by affecting key genes and signaling pathways.

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

A Jordanian family with Clouston syndrome has a common GJB6 gene mutation.

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

The Yorkshire terrier has a genetic hair loss condition not improved by treatment.

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

A Holstein calf in Iran with a severe genetic skin disorder was euthanized due to incurable symptoms.

Hair problems can be caused by genetics or the environment, and treatment should focus on the cause and reducing hair damage.

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

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Most hair loss in children is caused by a few common conditions, and it's important to diagnose these properly and support the child's mental health.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

Histone demethylases play a key role in the development of many diseases and may be targets for treatment.

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.

Recent progress has been made in understanding inherited hair and nail disorders.

A new mutation in the Connexin 26 gene was found in a patient with KID syndrome, expanding the known disorders linked to this gene.

Hair thinning causes stem cell loss through a process involving Piezo1, calcium, and TNF-α.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

Understanding how acne develops in different diseases could lead to new treatments.

The most common cause of hair loss in children is tinea capitis, followed by alopecia areata and telogen effluvium.

Latisse (bimatoprost 0.03%) is widely used in dermatology but the document doesn't give detailed evidence or numbers.

Bimatoprost helps with hair growth and eye conditions but can be costly and have side effects.

Monilethrix causes different levels of hair loss in family members.

A protein called PCBP2 controls the production of a hair growth protein by interacting with its genetic message and is linked to hair loss when this control is disrupted.

Disrupted stem cell signals in hairpoor mice cause hair loss.