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The article concludes that a thorough diagnosis and treatment plan, including medications, non-invasive methods, or surgery, is important for managing hair loss, with a combination of minoxidil and finasteride being particularly effective.

Hoxc13 gene affects wool length in Gansu alpine fine-wool sheep.

The document concludes that each reviewed medical book is useful for its specific area in pediatric care, especially the "Neonatal Formulary" for neonatal drug information.

The document explains hair and nail biology, common hair loss conditions and treatments, oral and genital skin diseases, and the risks and treatments associated with squamous cell carcinoma.

Three dogs with a rare skin condition improved with treatment.

Mice with extra human KLK14 had hair and skin problems, including weaker cell bonds and inflammation, linked to Netherton syndrome.

Regulatory γδ T cells help protect hair follicles from alopecia areata and promote hair regrowth.

Improving maternal diets can prevent severe health issues, including death, from goiter in goat kids.

The document concludes that the girl's hairlessness is likely inherited from her parents.

Ayurveda's descriptions of genetic disorders align with modern genetic understanding.

Over 67 genes linked to ichthyosis help improve diagnosis and treatment.

A person was born with both a rare hairless condition and a type of birthmark, which is an uncommon combination.

Early treatment of children's hair loss, which can be caused by various factors, is important due to its emotional impact.

Eyelashes are important for looks and eye protection, and more people are treating sparse eyelashes; more research is needed to understand eyelash biology and improve treatments.

Recent progress has been made in understanding inherited hair and nail disorders.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

Malnutrition can cause unusual eyelash growth and hair loss.

Oral minoxidil shows promise in treating monilethrix-related hair loss.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

Indian dermatologists recommend treating common hair loss with a balanced diet, stress reduction, mild shampoos, and sometimes minoxidil and supplements.

Guidelines for diagnosing common hair loss include detailed history, clinical examination, and various diagnostic techniques.

Buschke-Ollendorff syndrome is a rare genetic disorder causing skin and bone changes, with some cases also showing ADHD or developmental delays.

B6.Cg-Tyr c−2J Hr hr /J mice have a stronger delayed sunburn reaction and are good for UV research.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

Researchers found a new mutation in the LIPH gene of a woman with a rare hair condition.

Mutations in the KRT85 gene cause hair and nail problems.

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

Acitretin helped improve hand mobility and skin condition in a patient.

Some congenital hair disorders improve in childhood or with treatments like minoxidil and retinoids, while others like Netherton syndrome and trichothiodystrophy have a poor prognosis.

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