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A 6-year-old boy with autism improved his thyroid function and growth after addressing iodine deficiency caused by picky eating, but his psychiatric symptoms and picky eating continued.

A 27-year-old with APS-1 showed improvement in symptoms after treatment.

A cat with a rare pancreatic tumor and diabetes died despite treatment, showing similar symptoms to a human condition.

Looking at skin can help find and treat serious diseases early.

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

Satoyoshi syndrome can cause hair loss and other serious health issues, and is hard to diagnose.

A chest X-ray can effectively diagnose ectopic ACTH secretion from lung tumors.

The infant likely has Hay-Wells syndrome and needs genetic testing and heart screening.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

ACTH-dependent Cushing's syndrome linked to metastatic cervical cancer is rare and has high risks.

A new gene mutation linked to KID syndrome was found, expanding genetic knowledge.

Upadacitinib improved both Crohn's ileitis and alopecia universalis in a patient.

A man with multiple autoimmune diseases developed liver injury from azathioprine, but his liver improved after stopping the drug.

Olmsted syndrome is a rare skin disorder causing thickened skin and other symptoms.

Early diagnosis and personalized treatment for PCOS are crucial, especially for young women in West Bengal, India.

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

Albendazole and praziquantel can cause severe side effects, especially with prolonged use or liver issues.

A rare type of skin lymphoma was identified, affecting hair follicles and sweat glands.

Patients with ichthyosis often experience symptoms similar to psoriasis and atopic dermatitis, suggesting that targeted therapies could improve their condition.

Steroid treatment greatly improved the symptoms of a boy with a rare disorder called Satoyoshi syndrome.

The treatment for alopecia areata with diphenylcyclopropenone was unsuccessful.

Ovarian SAHA syndrome makes women with PCOS more resistant to insulin and increases their risk of blood sugar problems.

A Cavalier King Charles Spaniel had both uveodermatological syndrome and alopecia areata, and treatment with ciclosporin helped regrow hair.

COVID-19 may trigger severe skin flare-ups in people with autoimmune conditions like lupus.

A new ARID1B gene variation causes Coffin-Siris syndrome 1 and early high myopia in a Chinese family.

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.

The patient's long-term symptoms were due to Sheehan's syndrome, which improved with hormone therapy.

A man with both skin lesions and lung cancer improved quickly with chemotherapy, suggesting the skin condition might be a reaction to immune system injury.