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A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Not having enough or having too much of the protein Grainyhead-like 3 leads to various developmental problems.

A boy with progeria had eye problems and signs of aging like hair loss and skin wrinkling.

The document is a detailed medical reference on skin and genetic disorders.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

Finasteride and minoxidil are effective, low-risk treatments for male hair loss, and patient education on these therapies is important.

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

The document explains various skin conditions and their treatments.

Type 2 diabetes in youth is increasing, with high treatment failure rates and more severe than Type 1; certain drugs can lower lipid levels effectively with varying side effects, and apples may benefit heart health like statins but with fewer side effects.

Skin symptoms can indicate endocrine disorders and have various treatments.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

The document concludes that accurate diagnosis and understanding the type of hair disorder are crucial for treating hair loss in children.

Skin issues can indicate immune system problems.

There are many treatments for common hair loss, but more trials are needed to decide which are best.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Exosome treatment safely increases hair density in male patients with androgenetic alopecia.

Female pattern hair loss is different from male pattern hair loss and has unclear genetic causes.

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

FGF13 gene changes cause excessive hair growth in a rare condition.

A specific gene mutation causes Olmsted syndrome.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

Noggin gene inactivation causes skeletal defects in mice, varying by genetic background.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

EGFR and mTOR inhibitors may help manage Olmsted syndrome symptoms.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

Lichen planopilaris causes permanent hair loss and scarring due to damage to hair follicles and can be mistaken for other hair loss conditions.