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Tumor cell adhesion is linked to higher risk of SLN metastasis and melanoma recurrence, and a model including these factors predicts these outcomes better than one with just clinical data.

A man with kidney tumors and lung cysts was diagnosed with Birt–Hogg–Dubé syndrome and treated successfully, with genetic testing confirming the diagnosis.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Some immunosuppressed patients can get unusual skin infections from Malassezia, which can be treated with antifungal medication.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

Abnormal T-cells from thymomas cause non-motor symptoms in some myasthenia gravis patients.

A rare benign tumor was found in a man's scrotum, highlighting the need for accurate diagnosis.

Two women were diagnosed with a rare melanoma that looked like hair loss but was actually a type of skin cancer.

Suppressing the HGPS mutation may improve symptoms and suggest reversibility.

A 79-year-old man was diagnosed with a rare skin condition called nevus comedonicus on his eyelids.

Temporal triangular alopecia is a non-scarring hair loss in children, often linked to other health conditions.

A woman with undifferentiated connective tissue disease was diagnosed with renal amyloidosis and carpal tunnel syndrome.

Linear cutaneous lupus erythematosus on the scalp is rare, often affects young Asians, and can be treated with specific medications.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Acute leukemias with the Philadelphia chromosome may be biphenotypic, and identifying this is important for proper treatment.

A young woman had a rare scalp tumor usually found in older women.

Anti-SRP myopathy can be linked to systemic lupus erythematosus and may improve with specific treatment.

A unique type of lupus panniculitis causes reversible hair loss on the scalp in East Asians.

Multiple pilomatrixoma may indicate Turner syndrome.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

A genetic variant in the KRT71 gene may cause loose anagen hair and wooly hair, and symptoms might improve with age.

A specific gene mutation causes a rare hair loss condition in a Chinese patient.

SLE should be considered in unexplained fevers, even in males.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

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

SLE and DM can coexist but are rare and need careful evaluation.

Scalp skin condition LEDS has similar features to Zoon's balanitis, a mucosal skin disorder.

Postmenopausal frontal fibrosing alopecia may be a unique condition linked to postmenopausal changes.