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The man has a genetic skin condition called pachyonychia congenita.

A rare scalp condition with hair loss was correctly diagnosed and treated, leading to hair regrowth.

Inverted follicular keratosis on the eyelid can be cured with surgery and has a great prognosis.

Thorough evaluations and conservative management can lead to positive outcomes in pediatric adrenocortical carcinoma.

A postmenopausal woman had rare symptoms due to a possible ovarian tumor, needing thorough evaluation.

The method effectively reduces and hides scalp defects after surgery.

BMP2 needs periosteal tissue to help regenerate mouse middle finger bones within a specific time.

The new Mercedes flap variant effectively closed medium-sized scalp defects in a single operation with good cosmetic results and no complications.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

Isotretinoin and other medications showed promising results for treating a rare scalp condition linked to severe acne.

The surgery for severe congenital ptosis in children is safe and effective, with good long-term results.

A rare skin lesion in a 64-year-old woman was successfully treated with a laser, showing minimal redness and no return after one month.

Flexural follicular lichen planus is a rare skin condition affecting body folds.

A fungal infection can look like a different scalp condition in teens, leading to wrong treatment until proper tests are done.

Erosive pustular dermatosis is a rare skin disease that's hard to treat and affects the scalp or legs.

Inverted follicular keratosis can look like cancer but is actually a harmless tumor.

PRAME is often present in Paget disease and could help in diagnosis, but more research is needed.

A woman's masculine features were caused by a rare ovarian tumor that produced male hormones.

A long-term pubic rash was finally diagnosed as white piedra and cured with ketoconazole.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

TAF can be identified by excessive skin thickening and clogged hair follicles, helping distinguish it from similar skin conditions.

Cantú syndrome is caused by mutations in the ABCC9 gene.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Pigmented papules on the ear can be a rare skin condition called cutaneous amyloidosis, treatable with topical tretinoin.

The protein structures in the hair and tendon were preserved, but their molecular arrangements changed.

Chronic scalp lesions with crusts and pus indicate Erosive Pustular Dermatosis, which is confirmed by biopsy and effectively treated with strong topical steroids.

Pallister-Killian Syndrome is a complex genetic disorder requiring coordinated care and genetic counseling.

Lipedematous alopecia causes permanent hair loss due to increased scalp fat.

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.

Surgical removal of abnormal fat pads fixed the woman's eyelid issue caused by likely silicone injections.