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A Chinese family had a child with a specific gene mutation causing vitamin D-resistant rickets, but the child improved with calcium and low-dose calcitriol.

Two different mutations in the vitamin D receptor gene cause different symptoms and responses to treatment in Lebanese patients with hereditary rickets.

Hair loss in androgenetic alopecia is caused by genetic factors and androgen excess, and can be treated with combined therapies.

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

The book helps veterinarians understand and treat hair loss in animals.

The conclusion is that different types of hair loss in dogs and cats can be cosmetic or serious, and affected animals should not be bred.

CCCA is a scarring hair disorder mainly affecting people of African descent, needing better awareness and treatment.

Diabetes can cause a variety of skin disorders, some of which may signal more serious health issues.

The document concludes that early recognition and treatment of PCOS in adolescents is crucial for managing symptoms and long-term health risks.

Hair follicles offer promising targets for delivering drugs to treat hair and skin conditions.

Adrenal disorders can cause lasting brain and behavior issues in children.

Changes in keratin affect skin health and can lead to skin disorders like blistering diseases and psoriasis.

Researchers created a mouse model of a type of rickets that does not cause hair loss.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

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

Skin problems can be signs of hormone-related disorders and recognizing them early is important for treatment.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

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

Different types of hair loss in dogs and cats have various causes and treatments, with outcomes ranging from good to uncertain.

Alopecia in animals can be hereditary, congenital, or acquired, with treatments and outcomes varying widely.

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

Skin changes can help diagnose and manage endocrine disorders like thyroid problems, diabetes, and adrenal gland conditions.

Dermatoscopy is a useful tool for diagnosing hair disorders and can help choose samples for more detailed analysis.

The article explains the genetic causes and symptoms of various hair disorders and highlights the need for more research to find treatments.

Researchers found a gene mutation responsible for a rare hair loss condition.

In a Tuscan pediatric clinic, 7.19% of children had hair or scalp disorders, with nonscarring alopecia being the most common.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

The document concludes that hair analysis is not good for assessing nutrition but can detect long-term heavy metal exposure.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

New biopsy techniques and tools improve alopecia diagnosis, and both too much and too little selenium can cause hair loss.