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A patient with a scalp condition and benign skin tumor experienced hair loss and did not improve with treatment, choosing not to have surgery despite a small cancer risk.

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

Pediatricians should treat some hair loss types in children and refer others to a dermatologist.

Diagnosing and treating skin conditions is challenging, especially when drug reactions mimic other diseases.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

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

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

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

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.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

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

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

Triangular temporal alopecia is a benign hair loss pattern best diagnosed with dermoscopy, with limited treatment options like surgery and hair transplantation.

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."

Mutations in keratin genes cause cell fragility and various skin disorders.

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.

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

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

A girl with Becker's nevus syndrome showed good improvement in breast development using spironolactone.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.

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

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

The conclusion is that Pigmented Epithelioid Melanocytoma can start from hair follicle stem cells or from a mole on the skin.

A rare skin condition caused droopy and outward-turning eyelids in a patient.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

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

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

A rare skin disorder, nevus comedonicus, can appear on one side of the body following Blaschko's lines.

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