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Kidney transplant patients who had COVID-19 experienced a significant drop in their quality of life due to long-lasting symptoms.

Satoyoshi syndrome symptoms can improve with corticosteroids and surgery.

Some skin diseases and anaemia are related, and treating the skin condition can often improve the anaemia.

Most skin conditions in Down syndrome are benign and involve dry or thickened skin.

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

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

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

DAVID syndrome is a condition with immune system and hormone deficiencies, needing early diagnosis to avoid serious complications.

Satoyoshi syndrome can cause eye problems like uveitis and retinal vein issues.

Children's screen time increased during the pandemic, causing various health issues.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Lack of Cisd2 disrupts calcium balance in cells, leading to poorly functioning neutrophils.

The patient was diagnosed with celiac disease after a long delay, showing the need for better awareness and earlier detection.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The removed ovarian tumor was a rare type of blood vessel tumor that improved the patient's symptoms and hormone levels after surgery.

Doctors should know how to diagnose and treat PCOS, which often involves checking for high male hormone levels and using medications to manage symptoms.

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

Sheehan's syndrome can sometimes cause psychosis.

Some drugs can cause skin reactions, which may improve when the drug is stopped, and rapid diagnosis and stopping the drug is crucial.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

Shock can be an early sign of Autoimmune Polyendocrine Syndrome Type II.

PCOS is a hormonal disorder affecting many women, leading to symptoms like acne and irregular periods, and increasing the risk of diabetes and heart disease.

Mutations in the SHH pathway in certain skin cells can cause skin tumors and abnormal hair growth.

Non-classic congenital adrenal hyperplasia (NCCAH) can mimic PCOS and requires genetic testing for proper diagnosis and treatment.

Female relatives of PCOS patients have a higher chance of showing PCOS symptoms.

Norethisterone (jenapharm) therapy is effective for endometrial cancer.

Autoimmune and metabolic issues are linked, and treating one may worsen another.

ACTH may be an effective first-line treatment for acute calcium pyrophosphate crystal arthritis.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

A 29-year-old woman with symptoms of both lupus and rheumatoid arthritis improved with specific medications.