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EPDS is a rare, chronic scalp condition that's hard to treat and needs better awareness for improved outcomes.

A guinea pig with ovarian cysts had a uterine infection and abnormal uterus lining due to a piece of hay inside it.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

Bone marrow and hair follicle cells help form skin tumors, suggesting new treatment targets.

ECCL should be considered in patients with specific skin and eye lesions.

A 19-year-old man had a rare skin condition on one side of his face that looked like another skin disease.

Nevus comedonicus can appear later in life and affect both eyelids.

Cystic panfolliculoma resembles hair follicle tumors due to specific cell interactions.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Castor oil-based polyurethanes are promising for making safe, strong-performing, eco-friendly hair-styling products.

Early diagnosis of trachyonychia improves treatment and reduces psychological and cosmetic issues.

Dermoscopy helps accurately diagnose and treat benign skin cysts.

Some cases of tinea capitis, a fungal scalp infection, can look like scarring hair loss due to the body's immune response and the fungus itself.

Most adrenal cortex tumors are benign and non-secreting, but proper diagnosis and treatment are important due to the rare possibility of cancer.

A high school wrestler's skin rash was cured with antifungal medication after a misdiagnosis and incorrect treatment led to a fungal infection.

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

A 29-year-old man had a jaw plaque diagnosed as follicular mucinosis, linked to nestin-positive hair follicle stem cells.

Transcranial electrical stimulation with bisphosphonates helps maintain bone collagen better than bisphosphonates alone.

Porphyria cutanea tarda causes skin issues due to an enzyme deficiency.

Paraproteinemic keratopathy can show eye symptoms before other signs of disease, needing careful treatment and long-term follow-up.

A 16-year-old girl's skin rash was likely caused by an infection and improved with topical steroids.

A woman with a rare ovarian tumor and hyperparathyroidism improved after surgery, highlighting the need for reporting unusual cases to understand and manage rare diseases.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

Oral zinc gluconate and topical steroids significantly improved a rare scalp condition in three elderly patients.

A family had a rare fungal infection called white piedra, identified as Trichosporon inkin.

The document concludes that careful diagnosis is crucial for chromosome 13q deletion syndrome, tamoxifen can cause reversible eye damage, finasteride may be linked to cataracts, and OCT is useful for diagnosing macular diseases.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.