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Endocrine diseases in dogs often cause skin problems, with hypothyroidism and hyperadrenocorticism being common and leading to hair loss and infections.

The document concludes that understanding genetic mutations in the PI3K-AKT-mTOR pathway can lead to better diagnosis and treatment for certain genetic skin disorders.

Early diagnosis and treatment of Kaposi varicelliform eruption are crucial to prevent severe complications.

A man developed a rare skin condition after a hair transplant surgery.

AFM helps study hair surfaces for dermatology, cosmetics, and forensics.

Acitretin is effective for severe skin conditions but has significant side effects and requires careful monitoring.

We need to learn more about 5α-reductases and neuroactive steroids to safely make drugs targeting these enzymes.

The harlequin ichthyosis mouse mutation causes thick skin and early death, resembling a human skin disorder.

New gene variants linked to a rare inherited hair loss disorder were found in three Chinese families.

Hair microscopy is a simple and cost-effective method to help diagnose systemic diseases in children.

Enzymes called 5α-reductases have many body functions and need more research to safely use inhibitors.

Certain vitamins in wrong amounts, alcohol abuse, metals, and other toxins can cause serious brain and nerve damage.

Mice with alopecia areata had wider lymphatic vessels in their skin.

Non-classical 21 hydroxylase deficiency is an underdiagnosed cause of female hair loss and polycystic ovarian syndrome.

The 11th AICPE Congress in Rimini was a major event in European aesthetic plastic surgery.

Some lesser-known causes of PCOS include autoimmune issues, genetic mutations, and changes in the body's microbiome.

Mutations in the RBPJ gene cause Adams-Oliver Syndrome.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

Some hair loss disorders are caused by genetic mutations affecting hair growth.

Lash ptosis is more common and severe in people with congenital eyelid droop than in those with acquired eyelid droop or without eyelid droop.

Minoxidil cream can safely treat hair loss in kids with ectodermal dysplasia.

Women with nonclassic congenital adrenal hyperplasia experience more sexual dysfunction and distress.

A woman with a rare adrenal tumor and hormonal disorder had improved testosterone levels after surgery, but her menstrual irregularities continued.

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

Applying minoxidil can help improve hair growth in people with hair loss caused by LIPH gene mutations.

Women with congenital adrenal hyperplasia (CAH) have more sexual function issues than those with polycystic ovary syndrome (PCOS), but physical activity can improve sexual functioning in all women.

An 8-year-old girl had a rare, benign skin tumor on her forehead.

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