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The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

The study found that Keratosis Pilaris Atrophicans is a genetic skin condition that starts in childhood, involves inflammation and scarring, and current treatments are only somewhat effective.

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.

The report suggests a possible link between hair loss and hidden scalp tumors but states more evidence is needed to confirm this.

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.

The exam tested knowledge on various skin-related topics for CME credit.

New markers and pathways have been found in skin tumors, helping better understand and diagnose them.

Early detection of specific skin lesions can help identify Birt-Hogg-Dube syndrome and prevent serious complications.

A baby had a rare case of widespread milia, which was treated and is being monitored.

Scalp biopsies are important for diagnosing hair loss conditions.

Laser treatments are the most effective for porokeratotic adnexal ostial nevus.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

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

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

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.

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

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

The man was diagnosed with Cronkhite-Canada syndrome, a rare disorder with GI polyps, skin issues, hair loss, and nail problems.

A man's unusual scalp folds caused by a skin condition were treated with surgery and remained unchanged two years later.

Porokeratotic eccrine and hair follicle nevus is a very rare skin disorder possibly caused by a GJB2 gene mutation.

Hormone-replacement therapy improved a woman's skin condition known as lymphomatoid papulosis.

KFSD is a genetic disorder causing hair loss and skin issues, with no effective treatment.

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

The document says that treating the root cause of hair follicle damage is crucial to prevent permanent hair loss, and treatment options vary.

Minoxidil can cause severe skin reactions like Stevens-Johnson syndrome in rare cases.

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

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

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