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Scalp biopsies are important for diagnosing hair loss conditions.

A 15-year-old with KID syndrome developed a rare skin condition called PEHFN.

A woman showed neurological symptoms from psittacosis linked to bird exposure, improving after antibiotic treatment.

The document concludes that correct diagnosis of alopecia types is crucial, scalp biopsies are important, and more research is needed.

Most cases of Temporal Triangular Alopecia are found in early childhood and may be related to genetic conditions.

A man had a rare pigmented nodule on his scalp that developed from birthmarks.

Benign skin tumors need accurate diagnosis to ensure proper treatment.

The meeting highlighted the importance of genetic testing and multidisciplinary approaches in pediatric dermatology.

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

The conclusion is that accurately identifying folliculosebaceous tumors requires understanding their clinical signs and microscopic features.

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

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.

A woman had a unique skin growth with hair follicle, oil glands, fat cells, spindle cells, and nerve fibers.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

The chapter explains common scalp conditions, including infections, infestations, and tumors.

Eruptive vellus hair cysts are rare, benign skin lesions that are hard to treat.

First Korean case of Cronkhite-Canada syndrome with colon cancer and serrated adenoma.

Cronkhite-Canada syndrome can cause multiple gastrointestinal polyps and various physical symptoms.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

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

Basaloid follicular hamartoma's appearance can be similar to other skin conditions, and diagnosis should consider both the look and behavior of the tumor.

A 60-year-old man with Cronkhite-Canada syndrome improved with treatment, but the condition has a high mortality rate and a risk of colorectal cancer.

Cells from a skin condition can create new hair follicles and similar growths in mice, and a specific treatment can reduce these effects.

Hair loss in Cronkhite-Canada syndrome may be due to an autoimmune response.

A rare case of a benign hair follicle tumor with unusual skin changes highlights the need for timely diagnosis to prevent potential cancer.

Some skin tumors from hair follicles and glands can be linked to genetic syndromes and may be benign or malignant.

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

The study found that diseases can be grouped by symptoms and that the accuracy of predicting disease-related genes varies with the data source.

Spironolactone may help enlarge a small breast linked to Becker's nevus.

Topical vitamin D is useful for some skin conditions but not effective for others, and more research is needed.