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Putting calcipotriol ointment on the skin once doesn't change calcium levels in the body right away.

Dexamethasone-primed stem cell media shows promise in treating lupus by reducing symptoms and inflammation.

Satoyoshi syndrome is likely an autoimmune disease.

SH-SY5Y cell lysate is effective for diagnosing Satoyoshi syndrome.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

Mutations in the POC1A gene can cause a unique form of extreme insulin resistance and short stature.

Certain SPINK5 gene mutations are common in Israeli families with Comèl-Netherton syndrome.

Steroid pulse therapy improved symptoms in a man with Satoyoshi syndrome.

SSAT is a key enzyme affecting cell growth and metabolism, with potential but risky use in disease treatment.

A boy with a rare skin condition and kidney disease improved with cyclosporine after steroids failed, suggesting a new treatment approach.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Certain genetic changes in the LSS gene cause a rare skin and hair condition.

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Tacrolimus and corticosteroids can improve symptoms of Satoyoshi syndrome.

Overexpression of SSAT causes hair loss and skin issues, but reducing putrescine can help.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

Overexpression of SSAT in mice causes hair loss, liver damage, and sensitivity to polyamine analogues.

A new mutation in the ST14 gene causes a rare skin and hair disorder in a specific family.

Ets2 gene is crucial for placental development in mice.

Somatostatin analogues effectively manage ectopic ACTH syndrome when surgery isn't possible.

Increasing SSAT makes skin more prone to cancer.

A gene variant causes a skin and hair disorder by disrupting protein balance.

Mutations in the LSS gene cause a rare type of hereditary hair loss.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Cats can have hypersomatotropism without diabetes, suggesting current diagnosis methods may miss cases.

A 2-year-old girl had a hair disorder not shared by her identical twin.

One twin girl has Loose anagen syndrome with poorly anchored hair, diagnosed with a simple hair pull test, while her identical twin does not have the condition.

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

Trichostasis spinulosa mainly affects the nose, with many tiny hairs in one follicle, possibly influenced by hormones and sunlight.

Truncating mutations in the C2orf37 gene cause Woodhouse–Sakati syndrome.