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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.

Two boys had a rare skin condition needing to be differentiated from similar disorders, with unclear inheritance due to few cases.

Norfolk Terriers have a genetic skin defect causing scaling and blisters due to a keratin issue.

Dermoscopy helped diagnose a rare skin disease which slightly improved with treatment.

Acne keloidalis is a chronic skin condition on the back of the neck in young black men, needing surgery for severe cases.

Inflammation may cause nail issues in Cronkhite–Canada Syndrome.

Follicular mucinosis can be an early sign of aggressive mycosis fungoides.

Trichofolliculoma should be considered in children with scalp nodules for accurate diagnosis and treatment.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

A rare benign skin nodule was found on the buttock, a unique location for this condition.

A woman with cervical cancer had rare scalp metastasis causing a unique type of hair loss.

Onychomatricome is a benign nail tumor with specific dermoscopic features that help distinguish it from cancer.

Corticosteroids improved symptoms in a man with Cronkhite-Canada Syndrome.

Current treatments for neutrophilic alopecias in children are limited and often ineffective, especially for males and those of Afro-Caribbean descent.

Giant keratoacanthoma can look like squamous cell carcinoma, requiring careful diagnosis and surgical removal.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

A 54-year-old woman experienced progressive hair loss starting in adolescence, leading to sparse scalp hair and almost no eyebrows or eyelashes.

Dupilumab improved hair and skin in a woman with Netherton syndrome.

External factors like certain shampoos, bacterial infections, and parasites might cause hair defects similar to genetic conditions.

Early diagnosis and effective treatment of kerion Celsi prevent scarring and permanent hair loss.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

Merkel cells are abundant in facial vellus hair follicles, especially during the anagen phase.

A man with Cronkhite-Canada syndrome improved significantly with immunosuppressive therapy.

A woman had a rare skin condition with recurring painful nodules that heal in 6 weeks, often without needing treatment.

A man with severe leprosy developed painless ulcers and numbness, treated successfully with multiple drugs and vitamins.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

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