enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Osteogenesis imperfecta - Wikipedia

    en.wikipedia.org/wiki/Osteogenesis_imperfecta

    Osteogenesis imperfecta is a group of genetic disorders, all of which cause bone fragility. OI has high genetic heterogeneity , that is, many different genetic mutations lead to the same or similar sets of observable symptoms ( phenotypes ).

  3. Osteochondrodysplasia - Wikipedia

    en.wikipedia.org/wiki/Osteochondrodysplasia

    COL1A1/2-related osteogenesis imperfecta is inherited in an autosomal dominant manner. The proportion of cases caused by a De novo COL1A1 or COL1A2 mutations are the cause of osteogenesis imperfecta in the vast majority of perinatally lethal osteogenesis imperfecta, and progressively deforming osteogenesis imperfecta.

  4. Hypophosphatasia - Wikipedia

    en.wikipedia.org/wiki/Hypophosphatasia

    Osteogenesis imperfecta, congenital dwarfisms, skeletal dysplasias: Treatment: Asfotase alfa (Strensiq), an enzyme replacement therapy: Prognosis: Severe perinatal forms are lethal without treatment; adult forms may only show moderate symptoms: Frequency: Rare (1 in 100,000); [3] more common in some populations [4]

  5. Thanatophoric dysplasia - Wikipedia

    en.wikipedia.org/wiki/Thanatophoric_dysplasia

    Note: Prenatal ultra-sound images of the ribs sometimes appear asymmetrical when in fact they are not. In certain cases, this has caused a misdiagnosis of osteogenesis imperfecta (OI) type II. [citation needed] An unusual head shape called kleeblattschaedel ("cloverleaf skull") can be seen with type 2 thanatophoric dysplasia. [5]

  6. 'Jay & Pamela': Meet TLC's Newest Couple With the Same ... - AOL

    www.aol.com/jay-pamela-meet-tlcs-newest...

    On March 4, viewers will officially meet Jay Manuel, 28, and Pamela Chavez, 30, who have a condition called Osteogenesis Imperfecta Type 3 (OI) that causes brittle bones.

  7. Atelosteogenesis type I - Wikipedia

    en.wikipedia.org/wiki/Atelosteogenesis_type_I

    Causes. This condition is caused by mutations in the filamin B gene. [4] [5] [6] ... Osteogenesis imperfecta; Roberts syndrome; Short-rib polydactyly syndrome;

  8. List of fetal abnormalities - Wikipedia

    en.wikipedia.org/wiki/List_of_fetal_abnormalities

    Fetal abnormalities are conditions that affect a fetus or embryo, are able to be diagnosed prenatally, and may be fatal or cause disease after birth. They may include aneuploidies, structural abnormalities, or neoplasms. Acardiac twin; Achondrogenesis; Achondroplasia

  9. Bone fracture - Wikipedia

    en.wikipedia.org/wiki/Bone_fracture

    A bone fracture may be the result of high force impact or stress, or a minimal trauma injury as a result of certain medical conditions that weaken the bones, such as osteoporosis, osteopenia, bone cancer, or osteogenesis imperfecta, where the fracture is then properly termed a pathologic fracture. [3]