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  2. Category : Congenital disorders of musculoskeletal system

    en.wikipedia.org/wiki/Category:Congenital...

    Generally, diseases outlined within the ICD-10 codes Q65-Q79 within Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities should be included in this category. Wikimedia Commons has media related to Congenital diseases and disorders of musculoskeletal system .

  3. Category:Congenital disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Congenital_disorders

    This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes Q00-Q99 within Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities should be included in this category.

  4. Constriction ring syndrome - Wikipedia

    en.wikipedia.org/wiki/Constriction_ring_syndrome

    Constriction ring syndrome (CRS) is a congenital disorder with unknown cause. Because of the unknown cause there are many different, and sometimes incorrect, names. It is a malformation due to intrauterine bands or rings that produce deep grooves in (most commonly distal) extremities such as fingers and toes.

  5. Birth defect - Wikipedia

    en.wikipedia.org/wiki/Birth_defect

    Birth defects are divided into two main types: structural disorders in which problems are seen with the shape of a body part and functional disorders in which problems exist with how a body part works. [3] Functional disorders include metabolic and degenerative disorders. [3] Some birth defects include both structural and functional disorders. [3]

  6. Fetal warfarin syndrome - Wikipedia

    en.wikipedia.org/wiki/Fetal_warfarin_syndrome

    Fetal warfarin syndrome is a disorder of the embryo which occurs in a child whose mother took the medication warfarin (brand name: Coumadin) during pregnancy.Resulting abnormalities include low birth weight, slower growth, intellectual disability, deafness, small head size, and malformed bones, cartilage, and joints.

  7. Roberts syndrome - Wikipedia

    en.wikipedia.org/wiki/Roberts_syndrome

    Roberts syndrome, or sometimes called pseudothalidomide syndrome, is an extremely rare autosomal recessive genetic disorder that is characterized by mild to severe prenatal retardation or disruption of cell division, leading to malformation of the bones in the skull, face, arms, and legs.

  8. Uterine malformation - Wikipedia

    en.wikipedia.org/wiki/Uterine_malformation

    See Triplet-birth with Uterus didelphys for a case of a woman having spontaneous birth in both wombs with twins. Class IV— Bicornuate uterus (uterus with two horns). Only the upper part of that part of the Müllerian system that forms the uterus fails to fuse, thus the caudal part of the uterus is normal, the cranial part is bifurcated.

  9. Proximal femoral focal deficiency - Wikipedia

    en.wikipedia.org/wiki/Proximal_femoral_focal...

    There are typically four classes (or types) of PFFD, ranging from class A to class D, as detailed by Aitken. [4] [5]Type A — The femur bone is slightly shorter on the proximal end (near the hip), and the femoral head (the ball of the thigh bone that goes into the hip socket) may not be solid enough to be seen on X-rays at birth, but later hardens (ossifies).