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A woman with acromegaly experienced severe hair loss from a drug called Lanreotide Autogel, which improved after stopping the treatment.

A man with rare skin changes on his fingers was diagnosed with multiple myeloma-linked amyloidosis.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

Pygmy goats with seborrhoeic dermatitis showed skin symptoms and temporary improvement with corticosteroids, but the cause and inheritance of the disease remain unknown.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Kennedy's disease leads to muscle weakness and sensory issues, has no cure but manageable symptoms, and future treatments look promising.

Some psychiatric medications can cause reversible hair loss.

Vitamin D Dependent Rickets Type-2A can cause complete hair loss and bone growth issues in infants.

Both lasers are equally effective and safe for treating freckles.

The research found genetic differences in identical twins that could explain why one twin has a disease while the other does not.

Non-motor symptoms in myasthenia gravis are common and need early diagnosis for better management.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Electrical stimulation with a low-calorie diet reduces appetite, weight, and blood pressure in obese people with sleep apnea.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

Surgical removal of abnormal fat pads fixed the woman's eyelid issue caused by likely silicone injections.

Plica neuropathica can be a sign of schizophrenia and improves with antipsychotic treatment.

A toddler with unusual hypothyroidism symptoms improved with levothyroxine treatment.

Excessive selenium from a supplement caused toxicity but patients recovered with care.

A rare calcium deposit condition was found on a man's scalp.

A woman with lupus and Kikuchi-Fujimoto disease improved with treatment.

Hair loss was likely caused by gymnastics activities on a balance beam.

The study found no common cause for a girl's crystalline cataract and uncombable hair, suggesting their co-occurrence might be coincidental.

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

Finasteride helps treat eyelid spasms.

A rare skin condition usually found near the eyes was found on a farmer's scalp.

A boy with toxic shock syndrome had severe heart rhythm problems but recovered with treatment.

Recognizing minor skin lesions can help identify serious cancer syndromes.

Genetic testing is crucial for diagnosing and treating acrodermatitis enteropathica effectively.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

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