Search results
Results From The WOW.Com Content Network
This type of procedure is used for all Wassel types of polydactyly and is the most commonly used technique. It is recommended in all cases of thumb duplication with a hypoplastic, less-functional thumb. Otherwise, one could consider the Bilhaut-Cloquet. The ulnar thumb is preferably preserved as it is the more developed one in most cases. [12]
Approximately one third of individuals born with Carpenter syndrome have a type of heart defect. Commonly seen heart defects may include: narrowing of the pulmonary artery, transposition of the major blood vessels, or the presence of an abnormally large vena cava, which delivers blood back to the heart from the head, neck, and upper limbs.
Brachydactyly type D, also known as short thumb, [3] [1] stub thumb, [5] [6] or clubbed thumb, [5] [6] is a genetic trait recognised by a thumb being relatively short and round with an accompanying wider nail bed. The distal phalanx of such thumbs is approximately two-thirds the length of full-length thumbs.
Dr. Ahmed Badruddin, the baby's doctor, says that the boy has a full head of hair and very large ears. In addition to only having one eye, the baby has a number of other deformities on his body.
Saethre–Chotzen syndrome (SCS), also known as acrocephalosyndactyly type III, is a rare congenital disorder associated with craniosynostosis (premature closure of one or more of the sutures between the bones of the skull). This affects the shape of the head and face, resulting in a cone-shaped head and an asymmetrical face.
The mother was expecting triplets, but ended up delivering twins — one of which seemed to have absorbed extra limbs from the third unborn fetus. Doctors in India are stunned by baby born with 4 ...
Brachydactyly may also be a signal that one is at risk for congenital heart disease [1] due to the association between congenital heart disease and Carpenter syndrome and the link between Carpenter syndrome and brachydactyly. [2] Nomograms for normal values of finger length as a ratio to other body measurements have been published.
Klippel–Feil syndrome (KFS), also known as cervical vertebral fusion syndrome, is a rare congenital condition characterized by the abnormal fusion of any two of the seven bones in the neck (cervical vertebrae). [1]: 578 It can result in a limited ability to move the neck and shortness of the neck, resulting in the appearance of a low hairline ...