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A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

Advancements in liver cirrhosis treatment and prognosis could improve patient care.

Trichostasis spinulosa can look like acne but usually affects adults, not children.

A man with Klinefelter syndrome had a leg ulcer that didn't heal well, even with treatment.

Trichothiodystrophy causes unusual hair and developmental issues.

Proper training, techniques, and communication reduce risks and legal issues in digestive endoscopy.

A man developed male breast cancer after four years of finasteride treatment for an enlarged prostate.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

A specific gene change plus an additional mutation in the same gene cause hereditary trichilemmal cysts.

A newborn girl had a rare case of salivary gland tissue on her chest, which was safely removed.

Dermoscopy improves diagnosis and treatment planning for trichostasis spinulosa.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Using a special knife helps improve hairline scars from surgery.

Pili torti hair is fragile due to loose keratin filaments and weak disulfide bonds.

Amyand's hernia treatment is complex and depends on literature and surgeon's experience.

Quick diagnosis and biotin treatment can dramatically improve biotinidase deficiency symptoms.

HLA can be linked to autoimmune hepatitis.

The boy likely has a fungal infection causing hair loss.

Deoxycholic acid is FDA-approved for reducing submental fat, but its mechanisms are not fully understood.

An 18-year-old boy had a harmless skin nodule near his nose with hair and oil glands inside.

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

A woman had a cyst in her salivary gland, likely from Botox, which was removed and confirmed as an epidermoid cyst.

A new method using a Foley catheter on a ureteroscope makes difficult urethral catheterization easier and more effective.

A man with KID syndrome developed a rare cancer in a long-term skin infection.

New findings suggest the protein linked to Birt–Hogg–Dubé syndrome is important in cell signaling and could affect treatment understanding.

A newborn with severe low blood sugar due to a genetic issue needed major surgery after standard treatments failed.

A 15-year-old boy's skin and hair condition worsened due to improper treatment, leading to severe health issues.

Patients with both connective tissue disease and acid reflux are more likely to have certain symptoms and physical signs.

Trichotillomania can cause severe complications like hairballs in the stomach, needing surgery and psychiatric care.

A 66-year-old woman with skin lesions and other symptoms improved after treatment for porphyria cutanea tarda.