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COVID-19 causes more taste, smell, hair, memory, and concentration issues than other respiratory infections.

A 90-year-old man was diagnosed with heart failure due to wild-type transthyretin cardiac amyloidosis.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Reticular erythematous mucinosis syndrome can occur with minimal mucin deposition.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

The study identified five types of long COVID symptoms and suggests tailored management strategies for each.

The patient recovered well and returned to college without any lasting issues.

A baby with KID syndrome died from infections and organ failure at 18 months old.

The medicine Cyclosporin A might cause excessive hair growth by reducing a protein that controls hair growth.

Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

A TNFAIP3 gene mutation can cause unusual and varied symptoms of lupus and Sjogren's syndrome.

Rapunzel syndrome is more common in Asian countries and requires early diagnosis, especially in Asian girls.

A man had bad reactions to a hair loss treatment called DNCB.

Immunotherapy for cancer caused a patient to develop a condition affecting hormone production, requiring ongoing hormone replacement therapy.

Secukinumab treatment may cause HBV reactivation and hair discoloration.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

Mutations in the DSG4 gene cause a severe form of brittle hair and skin issues.

Standard treatment for congenital erythropoietic porphyria was ineffective over five years.

The man's skin condition improved with sun protection and topical steroids, but UV exposure still caused flare-ups.

Women in Australia report different signs of facial aging compared to women in the US, UK, and Canada; men with Lichen planopilaris often have hormonal abnormalities and thyroid disease.

COVID-19 can cause different skin symptoms that may help with early diagnosis and show how severe the disease is.

CCCA and lichen planopilaris have similar histological features, making them hard to distinguish.

RCVS should be considered in thunderclap headaches, and MRA and DSA are better for diagnosis than CT angiogram.

Two siblings were diagnosed with Trichothiodystrophy, identified by brittle hair and low sulfur content.

Diagnose and manage CCCA with thorough history, exams, and labs; treat with anti-inflammatory agents, stress reduction, and stopping harmful hair practices.

Alopecia areata and polymyalgia rheumatica may be linked autoimmune conditions.

The letter suggests that the study's comparison group might have affected the results and calls for larger, more detailed future research.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

Idiopathic hirsutism is the most common cause, followed by PCOS, and insulin resistance should be checked in patients with acanthosis nigricans.