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Mice without the Sp6 gene have problems developing several body parts, including hair, teeth, limbs, and lungs.

Hair proteins in preschool children and their mothers could indicate developmental changes and health status.

Mothers have more hair proteins than their children, with age-related differences in protein patterns, and some proteins in hair could indicate early childhood development.

Hes1 protein is important for hair growth and regeneration, and could be a potential treatment for hair loss.

Researchers created a new mouse model for studying Citrullinemia Type I and similar conditions, showing symptoms and treatment responses like those in humans.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

Researchers created a mouse with the same mutation as humans with trichothiodystrophy, showing similar symptoms and confirming the condition is due to defects in DNA repair and gene activity.

An 8-year-old Saudi boy was diagnosed with a rare genetic disorder causing hair loss, skin issues, and light sensitivity.

Over half of the children had abnormal hair under a microscope, with many having genetic hair conditions.

Iron deficiency may be related to hair loss, but there's not enough evidence to recommend iron screening or supplements for all hair loss patients.

The document concludes that the exact way alcohol causes harm to fetal development is unknown, but it significantly affects nutrient transport to the fetus and a safe level of alcohol during pregnancy is not determined.

Finasteride caused blisters on hands and feet.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

Biotinidase deficiency has various symptoms and can be treated with biotin supplements.

Eating disorders like anorexia and bulimia cause skin problems, and dermatologists can help detect these disorders early for better treatment outcomes.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Valproic acid can cause muscle damage and liver issues, which improve after stopping the drug.

Injecting triamcinolone into the eyebrow area may help eyelash regrowth in alopecia areata patients.

2% minoxidil solution improved hair density and quality in children with Loose Anagen Hair Syndrome.

Genetic testing confirmed a young girl has Atrichia with Papular Lesions due to mutations in the hairless gene.

The report shows a young man with Hutchinson-Gilford Progeria Syndrome had typical and additional eye problems related to the disease.

A baby had a unique skin condition with a pale patch and surrounding dark hairs, not linked to other health issues.

No effective treatment exists to stimulate hair growth in atrichia with papular lesions.

Transverse sections are better for non-scarring hair loss, vertical sections are better for lichen planopilaris, and either method works for other scarring hair loss types.

Adrenal disorders can cause lasting brain and behavior issues in children.

FOXN1 gene mutations cause a rare, severe immune disease treatable with cell or tissue transplants.

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

A girl with a rare syndrome had successful hair loss treatment with no relapse after 4 years.