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The document concludes that managing skin conditions during pregnancy is important and requires specialized care.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Skin issues can indicate immune system problems.

Hair growth-related cells need the enzyme SCD1 to help maintain the area that supports hair growth.

Accurate diagnosis and tailored treatments are crucial for managing hair loss in humans and animals.

The research found that people's hair proteins vary, especially by ethnicity and body part, which could help identify individuals in forensic science.

The research found that people's hair proteins vary by individual and body part, with some differences between ethnic groups, which could help in forensics.

Early diagnosis and lifelong zinc supplementation are crucial for treating acrodermatitis enteropathica effectively.

Treating non-classic congenital adrenal hyperplasia is complex because the benefits of hormone treatment must be weighed against potential health risks.

Testosterone undecanoate safely and effectively increased penis size in male children with 5-alpha-reductase deficiency.

A 6-year-old girl was diagnosed with a rare hair disorder and started treatment with topical minoxidil.

Understanding genetic mutations helps diagnose and treat skin disorders like ichthyosis.

Baricitinib reduces inflammation and improves cell health in premature aging cells.

Botanical extracts and Minoxidil improved hair condition in a boy with a genetic disorder.

Dupilumab helped improve skin and prevent new lesions in a child with a rare immune disorder and severe eczema.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

The document talks about hard-to-treat and rare acne types, their connection with other health issues, the importance of correct diagnosis, and the challenges in managing them.

Genetic variants in PDE6H and LPAR6 cause vision impairment and hair loss in two Pakistani brothers.

Mutations in specific keratin genes cause improper hair structure in mice due to faulty keratin protein assembly.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

Certain genes on chromosomes 6, 10, 16, and 18 may increase the risk of alopecia areata.

Keratosis pilaris is often linked to genetic mutations and causes skin and hair abnormalities, regardless of those mutations.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

EDA signaling is linked to skin disorders, various cancers, and liver disease.

Early diagnosis and tailored treatments are crucial for managing ichthyosis syndromes with hair abnormalities.

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