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A new mutation in the HR gene is linked to a rare form of hair loss with limb deformities.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

A woman's male-pattern facial hair growth was caused by a rare malignant ovarian tumor that was difficult to diagnose and treat.

Lupus nephritis can cause severe kidney and blood vessel problems.

The woman was misdiagnosed with Graves Disease, leading to incorrect treatment, while she actually had Pituitary Resistance to Thyroid Hormone.

Diagnosing both systemic lupus and hemoglobinopathy is challenging due to overlapping symptoms.

Uncombable hair is inherited dominantly with complete penetrance.

People with Mucopolysaccharidoses often have skin problems like thick skin and extra hair, and recognizing these can help diagnose and treat the condition early.

Advanced imaging techniques are crucial for accurately diagnosing Monilethrix, a rare hair disorder.

The research found that MRI and certain hormone levels can help tell apart ovarian tumors from hyperthecosis in postmenopausal women, but tissue analysis is still needed for a definite diagnosis.

RHUPUS should be considered in children with deforming arthritis.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

A young woman had a rare scalp tumor usually found in older women.

Tigason improved hair growth in a boy with monilethrix without side effects.

Immunocompromised patients can develop skin and hair issues due to a virus.

The study found that certain microRNAs are higher in the cells and lower in the fluid of women with a specific type of polycystic ovary syndrome, and one microRNA could potentially help diagnose the condition.

Taking tamsulosin or finasteride and being older increase the risk of floppy iris during cataract surgery.

A rare type of skin cancer with mucosal involvement was partially treated but eventually relapsed.

A woman with breast cancer developed a rare condition causing excessive fine hair growth on her face and body.

A genetic defect causes males in some Mediterranean populations to be born with ambiguous genitalia and develop male traits at puberty.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Topical minoxidil can help improve hair in trichonodosis.

A miner developed extra shoulder hair due to long-term work pressure and inflammation.

An unusual growth of Leydig cells in a woman's ovaries caused her excessive hair growth, which was treated successfully with surgery.

Atrichia with papular lesions causes irreversible hair loss from infancy and is often misdiagnosed.

Trichilemmal carcinoma shares genetic changes with other skin cancers, suggesting similar causes and potential treatments.

Tofacitinib significantly improved symptoms in a patient with overlapping autoimmune disorders.

Recognizing LET and AITD can help diagnose SLE early for better treatment.

TB lymphadenitis can occur in people with SLE on long-term immunosuppressive therapy.