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Early diagnosis of Trichorhinophalangeal syndrome type 1 is crucial for treatment and was achieved through clinical examination and family history.

Dental pulp stem cells are better for tissue repair, while fat tissue stem cells may be more suited for wound healing and hair growth.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Scientists have developed a new method using stem cells to grow and transplant hair follicles, which could be useful for hair regeneration treatments.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Congenital triangular alopecia is a hair loss condition present from birth or early childhood with no effective treatment needed.

An 11-year-old boy in Saudi Arabia has a rare case of hypoparathyroidism with severe brain calcifications but normal development and no known cause.

A 6-year-old boy developed excessive hair growth after taking diazoxide for low blood sugar.

5% topical minoxidil improves hair density and quality in monilethrix patients.

A specific mutation in the K25 gene causes a rare genetic disorder with curly hair at birth and later hair loss, along with dental issues.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Laser treatment and synovial fluid can change hair follicle cells to resemble joint cells, with the changes being more significant when both treatments are used together.

A boy's hair that was frizzy and hard to comb returned to normal after 9 months, possibly due to genetic factors.

Keeping β-catenin levels high in mammary cells disrupts their development and branching.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.

Herbal hair serum with natural ingredients can effectively treat common hair problems.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Platelet-Rich Plasma (PRP) treatment can significantly increase hair count and thickness in people with Androgenetic Alopecia (AGA) with minimal side effects.

The serum with hibiscus and other natural ingredients improves hair growth and quality.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requiring high doses of calcium and vitamin D for treatment.

A genetic mutation in the EDA gene causes hypohidrotic ectodermal dysplasia in cats.

A 14-year-old girl with a condition that makes her hair easy to pull out also has a hair-pulling disorder, and treatment helped but she relapsed after a year.

The wolves suspected of man-eating in the 1880s likely ate very little human flesh and mostly consumed a diet similar to herbivores and omnivores.

A child with a rare vitamin D-resistant condition improved with treatment.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

Jatropha dioica may have antiviral, antifungal, and other medicinal properties, but more research is needed.

Proper periodontal treatment with xenograft effectively manages aggressive periodontitis in SLE patients.

A person got uncombable hair syndrome from two copies of chromosome 1 from their mother.

Ads showing gradual change work better for people less focused on new beginnings, while ads showing immediate change work better for those highly motivated by fresh starts.