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A combined surgical approach by different specialists can effectively treat large birthmarks on the scalp.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

A rare skin condition was misdiagnosed as a harmless mole on a woman's eyelid.

A specific mutation known for causing cancer is also found to cause a skin condition in a young girl.

Certain gene variations may increase the risk of alopecia, and platelet-rich plasma treatment can improve hair density in those with hair loss; a rare case of facial Becker's nevus was linked to uneven beard growth.

A man's scalp hair loss was due to a combined melanocytic nevus and alopecia areata, suggesting a possible link between the two conditions.

A woman with CHILD syndrome showed skin abnormalities, and the report suggests CHILD nevus and NEVIL might be the same condition, highlighting the need for diagnosis for genetic advice.

The term "porokeratotic adnexal ostial nevus" is proposed to unify overlapping skin conditions involving eccrine and hair follicles.

High androgen levels and genetic factors likely cause Becker's nevus and related symptoms.

The boy's skin condition improved significantly with a specific ointment after other treatments showed only mild results.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

An adult with a rare skin condition improved with tazarotene treatment.

Taking photos of your own skin can lead to fewer skin biopsies for mole monitoring.

Sirolimus effectively reduces lesions and improves quality of life in Blue Rubber Bleb Nevus Syndrome with manageable side effects.

A 16-year-old boy had a rare case of Becker's nevus on his face and mouth.

The document explains the diagnosis and characteristics of woolly hair nevus and alopecia neoplastica.

Sebaceous glands are involved in various skin disorders, some treatable with medications like finasteride and minoxidil.

The document concludes that various childhood hair and nail disorders exist, some may improve on their own, and advances in genetics and immunology could enhance treatment and counseling.

An 8-year-old boy with Recklinghausen's Disease shows various symptoms and is from a family with close genetic ties.

Children's hair loss can have various causes, including infections, autoimmune issues, physical stress, nutritional problems, and genetic factors.

Different sebaceous gland diseases can be treated with medications, hormone therapy, or surgical methods.

Older men's scalp damage increases with age and sun exposure, a baby girl in the Philippines has Schimmelpenning syndrome, and thyroid screening is advised for children with hair loss and certain risk factors.

Hair loss in rural Indian children is often due to malnutrition, poor grooming, stress, and infections.

Different races and genders have unique skin and hair issues, requiring specialized care and more research for effective treatment.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

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 document lists common and scalp-specific lesions, emphasizing the need for hair restoration surgeons to recognize these and refer patients to a dermatologist if necessary.

The pandemic changed how often certain skin conditions were diagnosed.

CTA is often mistaken for AA but doesn't respond to steroids and may require hair transplantation.