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A man with four autoimmune diseases suggests a new category for multiple autoimmune syndrome.

A protein called lfTSLP is important in causing allergic and other skin diseases and could be a target for treatment.

Treating H. pylori infection might help cure alopecia areata.

The JAK/STAT pathway is important in cell processes and disease, and JAK inhibitors are promising for treating related conditions.

Physical activity, height, and smoking affect prostate cancer risk.

Hormone imbalances can cause specific skin changes, which may help in early detection of endocrine disorders.

People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

People with Lichen planopilaris are more likely to have certain autoimmune and endocrine disorders but less likely to have conditions like allergies and diabetes.

Azathioprine's effectiveness and safety require careful monitoring and more research, especially regarding its use with corticosteroids and the role of TPMT status in patients.

Skin symptoms can indicate endocrine disorders and have various treatments.

Children with diabetes often have skin problems, which can be better managed with good blood sugar control.

Lack of sleep in mice leads to prostatitis by reducing certain hormones and activating an inflammatory pathway, which can be temporarily fixed with normal sleep.

The cause of Frontal Fibrosing Alopecia is unclear, diagnosis involves clinical evaluation and various treatments exist, but their effectiveness is uncertain.

The document concludes that regenerating functional ectodermal organs like teeth and hair is promising for future therapies.

Male and female skin differ due to hormones, affecting conditions like hair loss, acne, and skin cancer, and suggesting a need for gender-specific treatments.

Topical spironolactone may help treat ocular graft-versus-host disease with minimal side effects.

Recognizing specific skin features helps diagnose and manage lupus erythematosus effectively.

Frontal fibrosing alopecia in families shows similar signs to individual cases and may have a genetic link.

Hair loss is common in autoimmune diseases and can be an early sign of the condition, often requiring prompt treatment to prevent permanent damage.

Understanding the genetics of rare inherited ichthyosis syndromes is key for better treatments and genetic counseling.

The guidelines advise against using testosterone and DHEA in women for most conditions due to safety and effectiveness concerns, but suggest considering testosterone for postmenopausal women with low sexual desire.

The document is a detailed guide on skin conditions and treatments for dermatologists.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.

Skin doctors should know about skin and kidney disease links to prevent serious kidney problems.

Long COVID causes a wide range of long-lasting symptoms that change over time and are hard to diagnose and treat.

Lack or blocking of SRD5a, a key component in hormone creation, can lead to conditions like pseudohermaphrodism and affect hair growth, bone mass, muscle strength, and reproductive health. More research is needed on its regulation from fertilization to adulthood.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Understanding skin structure and development helps diagnose and treat skin disorders.

Doctors should use a detailed patient history and physical exam to diagnose joint pain, and consult a rheumatologist early for suspected autoimmune diseases.

The Endocrine Society advised against routine testosterone therapy for women, citing a need for more research on long-term safety and a clear definition of androgen deficiency.