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A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Two rare genetic diseases cause severe rickets in children due to defects in vitamin D metabolism.

Mutations in the vitamin D receptor cause hereditary vitamin D-resistant rickets, leading to poor bone health and requiring high calcium doses for treatment.

Loss of a specific protein in skin cells causes symptoms similar to psoriasis.

Odontogenic keratocysts are caused by abnormal Hedgehog signaling and can lead to tooth and bone issues.

The document suggests a possible link between FAM111B gene mutations and increased cancer risk, particularly pancreatic cancer.

The cat's hypothyroidism was successfully managed with levothyroxine, leading to a stable condition.

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

A baby was diagnosed with IFAP syndrome due to a new genetic mutation, showing severe skin and developmental issues.

Rare ULBP3 gene changes may raise the risk of Alopecia areata, a certain FAS gene deletion could cause a dysfunctional protein in an immune disorder, and having one copy of a specific genetic deletion is okay, but two copies cause sickle cell disease.

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

Young adults who had liver disease as children often experience significant health problems and frequently need transplants.

Middle Eastern patients with epidermolysis bullosa show specific genetic mutations linked to different types of the disease.

A new gene mutation caused a man's rare skin condition, Schöpf-Schulz-Passarge syndrome.

Stem cell differentiation is crucial for skin barrier maintenance and its disruption can lead to skin diseases.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

A woman developed thick gums from everolimus treatment after a kidney transplant.

A patient's gum problems worsened after using cyclosporine for a scalp condition, but improved with a lower dose.

Early diagnosis and individualized treatment improve outcomes for Congenital Adrenal Hyperplasia.

Using skin grafts from behind the ear for oral surgery in two patients with jaw injuries led to successful healing and good results.

Some ovarian tumors can cause masculinization, and it's important to check for various causes when this symptom is present.

Finasteride may increase the risk of suicide or severe self-harm in men with mood disorders but not in the general population.

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

Dates may improve heart health, fight infections, protect kidneys, reduce inflammation, support pregnancy, promote dental and bone health, enhance mental function, and have anti-cancer properties, and are also beneficial for skin and hair care.

Survivors of Stevens-Johnson syndrome/toxic epidermal necrolysis need ongoing care for various long-term health problems.

New nano composite helps reduce scars and regrow hair during burn wound healing.

The conclusion is that using drugs to block the TOR pathway might slow aging and prevent age-related diseases.

Men taking dutasteride or finasteride have a slightly higher risk of developing type 2 diabetes.

Skin cell-derived vesicles can help heal skin injuries effectively.