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A specific ATR gene mutation is linked to a hereditary oropharyngeal cancer syndrome.

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.

To diagnose hair loss, use a systematic approach including history, exams, and tests.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

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

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

A new mutation in the ST14 gene broadens the understanding of ichthyosis-hypotrichosis syndrome.

Stopping forehead irritation and using hydrocortisone helped a man's skin, Martinique has lower melanoma rates, a man had an allergy to a specific antifungal, another had unexplained cysts, certain drugs can cause skin reactions without always being interrelated, a link between Fanconi anemia and a skin condition was suggested, high levels of a certain protein may play a role in a type of psoriasis, and there's a need to study the connection between scalp pain and hair loss.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

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 new PAX9 gene mutation causes missing teeth and hair problems, but not skin or nail issues.

Hair, teeth, and mammary glands develop similarly at first but use different genes later.

The STIM1 R304W mutation in mice leads to bone changes and teeth hair growth.

Different fish use the same genes to regrow teeth.

Mutations in the WNT10A gene can cause skin, hair, teeth, and other disorders, and may also affect other areas like kidney and cancer, with potential for targeted treatments.

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

WNT10A mutations often cause ectodermal dysplasias, with males showing more tooth issues than females.

A boy with GAPO syndrome had hair loss similar to male pattern baldness without hormone issues, possibly due to skin or blood vessel problems.

Light microscopy is useful for diagnosing different hair disorders.

The document concludes that early diagnosis and treatment are crucial for children with hair loss to prevent permanent damage, although not all conditions can be effectively treated.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

Scientists now better understand the genetics of hypohidrotic ectodermal dysplasia, leading to more accurate diagnoses and potential new treatments.

Hair and nails are similar keratin structures with different shapes and growth, affected by the same diseases and environmental factors.

NEMO syndrome and systemic lupus erythematosus are linked in a new disease association.

A 12-year-old girl in Saudi Arabia with Focal dermal hypoplasia showed skin and dental symptoms, highlighting the condition's variability and the need for personalized treatment.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

The TGF-β family helps control how cells change and move, affecting skin, hair, and organ development.

Ectodermal dysplasia causes various symptoms and early treatment is important for eye, dental, and skin issues.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.