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Osteogenesis imperfecta is dominant or recessive?
Osteogenesis imperfecta is typically inherited in an autosomal dominant pattern, meaning one copy of the mutated gene is enough to cause the condition. However, in some cases, it can be inherited in an autosomal recessive pattern if both parents are carriers of the mutated gene.
What part of the body is generally effected by osteogenesis imperfecta?
Osteogenesis imperfecta primarily affects the bones in the body, leading to brittle bones that are prone to fractures. It can also affect other connective tissues such as ligaments and tendons. Symptoms can vary widely depending on the type and severity of the condition.
Which type of cell appears first during osteogenesis?
Osteoprogenitor cells, also known as mesenchymal stem cells, are the first type of cell to appear during osteogenesis. These cells have the potential to differentiate into osteoblasts, which are responsible for bone formation.
A child has a knobby rib cage enlarged forehead and lower limbs are bent what is the diagnosis?
The symptoms described—knobby rib cage, enlarged forehead, and bent lower limbs—are indicative of a condition known as osteogenesis imperfecta (OI), commonly referred to as "brittle bone disease." This genetic disorder affects collagen production, leading to fragile bones, skeletal deformities, and distinctive facial features. The combination of these symptoms suggests a possible type of OI, which requires further clinical evaluation for confirmation and management options.
Why is the term limiting used to describe the limiting reactant?
The term "limiting" is used to describe the reactant that is completely consumed in a chemical reaction, thus limiting the amount of product that can be formed. It determines the maximum amount of product that can be produced based on its stoichiometry and quantity.
What countries are at risk of osteogenesis imperfecta?
USA
What calcuim does for the body?
Lack of calcium can lead to Osteogenesis Imperfecta
What causes blue sclerae in osteogenesis imperfecta?
Type I Osteogenesis Imperfecta is the most common and mildest type of this disease. In this type the Scleras (whites of the eyes) usually have a blue, purple, or gray tint.
What causes Craniotabes?
premature infants(as normal finding),rickets,osteogenesis imperfecta
Do you have to be born with osteogenesis imperfecta to have it?
Yes, because it is a genetic disease you inherit from your parents.
What is the difference between osteogenesis imperfecta and osteoporosis?
Osteoporosis occurs later in life and leads to weakening and fractures of the bones. Osteogenesis imperfecta is a congenital defect which causes fractures to occur from the slightest bump or touch in a child.
Where was osteogenesis imperfecta discovered?
Osteogenesis imperfecta, also known as brittle bone disease, was first described by British surgeon John F. Clarke in 1695. He observed patients with fragile bones that easily fractured, leading to the recognition of this genetic disorder.
What are some of the symptoms of osteogenesis imperfecta?
Osteogenesis imperfecta is a genetic disorder that causes brittleness of one bones. This can cause ones bones to break easily and even for no apparent reason. Also, it can lead to abnormally large amounts of repair tissue at the site of fractures.
Can babies be born with bone fractures or bone diseases causing them?
osteogenesis imperfecta - brittle bone disease
What is the medical term meaning poor development of bones?
Osteogenesis imperfecta means poor development of bones.
How tall can you be with osteogenesis imperfecta?
"some people may only grow to be three feet tall"sourcehttp://www.orthop.washington.edu/?q=patient-care/articles/arthritis/osteogenesis-imperfecta.html
What has the author Jenny Ford written?
Jenny Ford has written: 'An investigation into voice quality in eight individuals with osteogenesis imperfecta'
