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The patient has a rare skin condition that shows features of two known disorders.

The document reviews various hair and nail disorders, their causes, and treatments, emphasizing the need for proper diagnosis and the link between nail changes and systemic diseases.

Understanding normal hair growth and loss in children is key to diagnosing and treating hair disorders.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

A 21-year-old male has a benign skin condition called Becker's nevus, which he chose not to treat.

The document describes various skin conditions, their features, and treatments but lacks detailed study size information.

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

The document explains the genetic causes and characteristics of inherited hair disorders.

There is no standard treatment for the rare Cronkhite–Canada syndrome, which can be fatal and lead to cancer.

Shrinking skin cancer increases the chance of cancer in nearby lymph nodes.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Dermatopathology has made significant progress but many skin diseases remain incurable, requiring ongoing research.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

The meeting showcased rare skin disease cases, highlighting the need for accurate diagnosis and treatment.

Proper care and diet are crucial to prevent health issues in gerbils.

Cronkhite-Canada syndrome is rare, has a poor prognosis, and requires early diagnosis and ongoing treatment.

Thyroid disease can cause skin, hair, and nail problems, and treating the thyroid condition often improves these symptoms.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

The book details skin conditions in older adults, their link to mental health, cancer treatment importance, hair loss remedies, and managing autoimmune and itchy skin.

Eruptive vellus hair cysts are rare and often misdiagnosed, requiring biopsy for accurate diagnosis.

The document explains how hair follicles develop, their structure, and how they grow.

Iron deficiency might contribute to hair loss in women.

The document concludes that treatments for cicatricial alopecia are not well-supported by evidence, but hair transplantation shows more predictable and satisfactory results.

Botulinum toxin type A significantly reduces scalp psoriasis severity compared to placebo.

Advancements in tissue engineering show promise for hair follicle regeneration to treat hair loss.

Looking at skin can help find and treat serious diseases early.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

Eye exams are crucial for kids with 13q deletion syndrome, tamoxifen can cause vision loss, Propecia may lead to cataracts, Lipoid Proteinosis causes skin bumps, and OCT is useful for diagnosing macular diseases.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.