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An elderly woman's upper lip lump, thought to be a mucocele, was actually a rare type of lymphoma usually found on legs, treated successfully with chemotherapy and radiation.

Selenosis in calves causes health issues and changes in blood parameters.

Three related Persian cats have a rare, likely hereditary skin condition causing hair loss and poor coat quality, with limited treatment options.

Mild changes in bone markers relate to TCM syndromes in CKD-MBD patients.

Thorough evaluation and treatment are crucial for thyroid nodules.

A rare endocrine disorder, APS 1, was diagnosed in a 26-year-old man in Bangladesh.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Surgical excision is the best treatment for SCC.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

A woman with a new PTCH gene mutation has both Gorlin syndrome and severe hair loss.

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

Topical IKKα inhibitors may help prevent CCS tumours.

Drospirenone can hide symptoms of certain hormonal disorders, complicating diagnosis.

A 2-year-old girl with a rare vitamin D disorder had rickets and hair loss, but treatment was ineffective due to poor compliance.

People with PCNT mutations often develop severe insulin resistance and early-onset diabetes during childhood or adolescence.

A 9-year-old boy had a rare scalp condition usually seen in young men.

Early diagnosis and lifestyle changes are crucial for managing PCOD.

Upadacitinib may effectively treat both alopecia universalis and Crohn's disease.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

A calcified nodule on a boy's face came from hair follicles and expelled calcium through the skin.

A man with a weakened immune system was diagnosed with a rare skin condition called trichodysplasia spinulosa using skin examination techniques.

A new gene variant causes glucocorticoid resistance in a mother and son.

Chronic cutaneous lupus erythematosus should be considered when acne treatments don't work.

The document reports the first case of a rare skin condition in Colombia, the 19th case worldwide.

The boy's symptoms improved with vitamin C treatment, highlighting the need to consider scurvy in kids with unusual diets.

The young goat had anaplasmosis and copper deficiency.

Adult mice with CBS deficiency show minimal health issues and normal lifespan despite high homocysteine levels.

Patients with this syndrome can have different responses and worsening resistance to treatment over time.

The thyroid nodule was benign, and surgery was successful with a smooth recovery.

Stopping Cyclosporine A led to hair regrowth in a child with alopecia.