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The review suggests thorough evaluation and genetic testing for proper diagnosis and treatment of Chrousos syndrome.

The TCL1 transgenic mouse model is useful for understanding human B-cell leukemia and testing new treatments.

Recent genetic insights show that low-renin hypertension includes a range from essential hypertension to secondary or familial forms, affecting diagnosis and treatment.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The document concludes that stopping shaving or removing affected hair can alleviate Pseudofolliculitis barbae (PFB).

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Hair keratins evolved from ancient proteins, diversifying through gene changes, crucial for forming claws and later hair in mammals.

Mutations in the NR3C1 gene cause a rare condition that affects hormone signaling and can lead to various symptoms, with dexamethasone as a treatment option.

Hair microscopy is useful for diagnosing hair disorders, but clear definitions are needed for accurate genetic analysis.

Antiandrogenic drugs could be a good treatment option for frontal fibrosing alopecia.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

Damaged hair follicles make mice more prone to skin inflammation and skin cancer after UV exposure.

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

A 12-year-old boy with a rare genetic condition has progressive hair loss with no effective treatment.

Mechanical forces are crucial for shaping cells and forming tissues during development.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

Docetaxel, a chemotherapy drug, was reported to cause psoriasis in a patient for the first time.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

The Journal für Ästhetische Chirurgie expanded its board to improve collaboration and knowledge in aesthetic surgery.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

Researchers made a mouse model with curly hair and hair loss by editing a gene.

A boy with Pachyonychia congenita has a confirmed gene mutation, highlighting the need for a local genetic database in India.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

Chrousos Syndrome is caused by mutations that make the body less sensitive to glucocorticoids, leading to various symptoms and requiring high-dose treatment.

Mother and son diagnosed with a rare genetic hair loss condition with no effective treatment.

Researchers discovered potential origins and new treatments for skin cancer, including biomarkers for melanoma and therapies that reduce tumor growth.

An 86-year-old man with prostate cancer was diagnosed with a rare, low-grade breast cancer and underwent surgery but declined additional hormone therapy.

Scientists found key proteins and genes that affect skin and hair health, and identified potential new treatments for hair loss, skin disorders, and wound healing.

Peps help Arabidopsis plants grow more root hairs by affecting specific genes and calcium signaling.