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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.

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

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

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

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Some drugs can cause skin, nail, and hair problems, which are important for healthcare professionals to recognize and report.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

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.

Light microscopy is useful for diagnosing different hair disorders.

Skin changes can indicate hormonal imbalances and help diagnose endocrine disorders.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

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

Targeted cancer therapies often cause skin reactions, so dermatologists must manage these effects.

Early recognition and management of skin side effects from new cancer therapies can prevent treatment delays.

Hormone imbalances can cause skin diseases, and understanding these links is important for diagnosis and treatment.

Hair changes can indicate systemic diseases or medication effects.

Most HIV patients develop skin symptoms that can indicate the stage of their disease.

Different hair loss types need accurate diagnosis for proper treatment.

Taking vitamins, minerals, and amino acids can improve hair strength and quality in people with Monilethrix.

Some skin problems can be signs of diabetes or other metabolic diseases and recognizing them can help diagnose and treat these diseases early.

The nutritional supplement improved hair quality and reduced hair loss.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

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

Cats lose fur due to various reasons, including allergies, infections, genetics, hormones, diet, cancer, stress, and some conditions are treatable while others are not.

A child with trichothiodystrophy also had autoimmune thyroiditis and anemia, which is a new finding.

Endocrine diseases in children often cause skin changes like dryness, redness, acne, hair loss, and more.

The document concludes that understanding and managing hair loss in cancer patients is important, and more research is needed for better treatments.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

Thyroid problems can cause hair loss and change hair texture.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.