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A healthy woman got a chest abscess from a fungal infection after gallbladder surgery, which was treated but caused temporary hair loss due to the antifungal medication.

Horizontal sections of scalp biopsies are good for diagnosing Central Centrifugal Cicatricial Alopecia and help customize treatment.

SCD1 is crucial for skin health and overall energy balance.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Early diagnosis and genetic counseling are crucial for managing adrenoleukodystrophy.

Black women with CCCA are more likely to have uterine fibroids.

Calcitriol-resistant rickets is an inherited disorder that affects hair growth and causes hair loss.

A woman with a long-term skin condition developed a serious skin cancer that led to her death.

Selenium supplements can help improve symptoms and metabolic markers in lupus patients.

Pseudo-Cushing's symptoms disappear once the underlying issue is resolved.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

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

Non-coding RNAs may be key in diagnosing and treating rare skin disorders.

A new gene variant in a girl with Coffin-Lowry Syndrome may link the condition to early puberty.

CCCA can affect both genders and all ages, and it has a genetic component.

A rare case of scleredema in a diabetic woman showed loss of sweat glands, causing heat strokes, with treatment only slightly improving symptoms.

Vitamin B12 deficiency can cause skin darkening and other symptoms, which improve with B12 supplements.

Timely and aggressive treatment is crucial for improving outcomes in severe complications of adult-onset Still's disease.

Hidden sweat gland tumors might cause hair loss.

Autoimmune Polyendocrine Syndromes involve specific combinations of endocrine and non-endocrine autoimmune diseases.

Prenatal genetic diagnosis may not predict MELAS syndrome severity in offspring.

The N363S gene variant does not cause higher adrenal androgen levels in women with polycystic ovary syndrome.

Woman with diabetes had hair loss due to rare ovarian tumor; surgery improved hair growth.

Hormonal therapy is essential in late-diagnosed Kallmann's syndrome to prevent bone issues.

Elental is a good long-term treatment for Crohn's disease, similar to 6-mercaptopurine but with fewer side effects.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

BST2 protein and certain T cells increase in early alopecia areata.