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A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Minoxidil promotes hair growth but exact mechanism is unknown.

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

Bovines can have rare inherited skin diseases with specific symptoms like hair loss, fragile skin, and abnormal porphyrin buildup.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

The supplement highlighted advancements and challenges in plastic and reconstructive surgery, including the impact of smoking, chemotherapy, and new treatments like Tafluprost for hair loss.

Gene mutations can cause problems in male genital development.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

Nuclear Factor I-C is important for controlling hair growth by affecting the TGF-β1 pathway.

Genetic discoveries are key for understanding, diagnosing, and treating inherited hair and nail disorders.

Researchers identified specific genes that are important for mouse skin cell development and healing.

Women experience various skin issues at different life stages, requiring careful treatment and awareness.

Cosmetic surgery is more popular and cost-effective, but outcomes depend on the surgeon's skill and all procedures have potential complications.

Human skin's melanocytes respond to light by changing shape, producing pigments and hormones, which may affect sleep patterns.

The document emphasizes the importance of correctly identifying and classifying genetic hair disorders to help diagnose related health conditions.

Dutasteride-loaded nanoparticles coated with Lauric Acid-Chitosan show promise for treating hair loss due to their controlled release, low toxicity, and potential to stimulate hair growth.

CD61 is important for mouse tooth cell growth and works through Lgr5.

Children's hair loss can be caused by many factors, including autoimmune diseases, emotional stress, genetics, and infections, with treatment and prognosis varying.

Using cetirizine on the skin and taking vitamin D can help increase hair growth in children with hair loss from ectodermal dysplasia.

Hutchinson-Gilford Progeria Syndrome is a rare genetic disorder caused by a specific gene mutation, characterized by aging symptoms and managed by monitoring heart health and using low-dose aspirin.

Stopping finasteride can improve sperm count in infertile men.

A family was found with both Trichorhinophalangeal syndrome and Loose Anagen Syndrome, suggesting a genetic connection.

Fetal death was caused by umbilical cord stricture with hair growth in the Wharton jelly.

Ayme-Gripp Syndrome was confirmed in a woman through genetic testing, highlighting the need to consider rare genetic conditions in diagnoses.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

A girl with Becker naevus syndrome has a genetic variant in the ACTB gene related to her symptoms.

Rothmund-Thomson syndrome type 2 can cause chronic, poorly healing wounds.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Benzoyl peroxide and adapalene gels work differently to reduce acne in mice.