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A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

Researchers found a new mutation in the HR gene linked to a rare hair loss condition.

The hr gene is crucial for skin and hair health, with mutations causing hair disorders.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

The document concludes that periocular hair disorders have various causes and treatments, and proper evaluation by specialists is important for management and prognosis.

A girl with a rare skin condition called Keratosis Follicularis Spinulosa Decalvans showed no significant improvement with treatment.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

Some patients with mycosis fungoides or Sézary syndrome experience hair loss, which may be similar to alopecia areata or linked to skin lesions, possibly due to abnormal T cells, and bexarotene can help treat it.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The document is a detailed guide on skin conditions and treatments for dermatologists.

The document concludes that early diagnosis and treatment are crucial for managing skin diseases in ferrets.

New genetic mutations causing hair loss were found in a Chinese family.

A different gene near the hairless gene on chromosome 8p21 causes a rare hair loss condition in a German family.

A new mutation in the Hr gene causes hair loss in mice, similar to a human hair disorder.

The monkey's hair loss was due to an autoimmune disease, not genetics.

Certain mutations in a hair growth-related gene cause a type of genetic hair loss.

Hair ages and thins due to factors like inflammation and stress, and treatments like antioxidants and hormones might improve hair health.

Thyroid hormones affect skin texture, hair and nail growth, and can cause skin diseases related to thyroid problems.

Facial hair transplants are generally successful, with hair growth beginning around 3 months post-surgery.

Most Hairless gene mutations reduce its ability to work with the Vitamin D Receptor, which might explain a certain type of hair loss.

The document concludes that over 500 genes are linked to hair disorders and this knowledge is important for creating new treatments.

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

A boy and his father with hereditary hypotrichosis simplex were treated for hair loss, but the treatment result is unknown.

Marie-Unna Hereditary Hypotrichosis is a rare genetic condition causing sparse hair growth, requiring specific recognition for proper care.

Topical PUVA and tacrolimus ointment can effectively and safely treat infant alopecia universalis.

Hair diseases can have psychological effects and should be treated with a combination of psychosomatic care, therapy, and medication.

The first Japanese family with Marie Unna hereditary hypotrichosis showed hair condition improvement in a child and highlighted the risk of misdiagnosis.

Children's hair loss can be caused by various factors and should be treated with appropriate, age-specific methods and psychological support.