Search

everythinglearnresearchcommunity

for

Search:↓

Pharmacists play a key role in managing the use of anxiety medications and ensuring patients use them correctly.

BMP4 gene is crucial for hair follicle development in Liaoning cashmere goats.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

Children's screen time increased during the pandemic, causing various health issues.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

Skin healing from blisters can delay hair growth as stem cells focus on repairing skin over developing hair.

Combining minoxidil and plant extracts improved hair growth in a boy with a rare genetic disorder.

A KRT71 mutation in Hereford cattle in Uruguay causes thin, curly hair and scaly skin.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Hidradenitis suppurativa is a chronic skin condition more common in women, linked to genetics and lifestyle factors, and associated with various other health issues.

Hair loss in cancer patients can be related to the cancer itself, treatment, or other conditions, and understanding it is important for diagnosis and patient care.

Surgery to fix a broken upper arm bone can sometimes lead to nerve damage.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

Key genes crucial for sheep hair follicle development were identified, aiding fine wool breeding and human hair loss research.

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

ΔNp63α helps control a protein that stops cancer cells from spreading.

Passiflora incarnata may help with anxiety and sleep issues but has side effects; teleconsultation for heart failure can improve quality of life; increased screen time for children during the pandemic led to more clinical complaints; older and severely affected COVID-19 patients are more likely to have long-term symptoms.

The document concludes that Passiflora incarnata could help with anxiety, telemedicine might improve heart failure care, screen time for kids has increased, pregnant teens in Brazil are mostly okay with their body image, rare tuberculosis infection can occur after knee surgery, older and severely ill people are more likely to have long COVID-19 symptoms, HPLC might diagnose more diabetes cases, and psychiatrists should be involved in pain management.

European guidelines recommend regular eye and ear exams, skin care, vitamin D supplements, and cautious use of medications for managing congenital ichthyoses.

People with cleft lip and palate often have respiratory problems.

HPLC may detect prediabetes and diabetes earlier than Immunoturbidimetry because it shows higher A1c levels.

The patient with both scarring and non-scarring hair loss showed complex immune reactions and improved with steroid treatment.

The document concludes that understanding nail anatomy is key for diagnosing nail diseases, early signs of nail melanoma may allow for less aggressive treatment, and specific genetic mutations are important in thyroid cancer prognosis and treatment.

Non-scarring hair loss can be diagnosed with two 4mm punch biopsies, one cut vertically and the other transversely.

RET mutation is important in familial medullary thyroid carcinoma, and BRAF mutation in papillary thyroid carcinoma is linked to more aggressive cancer and higher death rates.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.

Madarosis is the loss of eyelashes and eyebrows due to various health issues and requires thorough examination to diagnose and treat the underlying cause.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

New gene identification techniques have improved the understanding and classification of inherited hair disorders.