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Plagiocephaly, also known as flat head syndrome, [1] [2] is a condition characterized by an asymmetrical distortion (flattening of one side) of the skull. A mild and widespread form is characterized by a flat spot on the back or one side of the head caused by remaining in a supine position for prolonged periods. [3]
Flat, asymmetric head and face [3] Head is typically cone-shaped (acrocephaly) or flat (brachycephaly) but can also be long and narrow (dolichocephaly) [4] Head is short from front to back [5] Lopsided face [4] Low-set hairline causing forehead to appear tall and wide [5]
Artificial cranial deformation or modification, head flattening, or head binding is a form of body alteration in which the skull of a human being is deformed intentionally. It is done by distorting the normal growth of a child's skull by applying pressure.
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.
She was the first baby born with the condition to undergo an operation to remove the second head. She died on February 7, 2004, after an 11-hour operation. [8] On March 30, 2004, Manar Maged was born. On February 19, 2005, 10-month-old Manar underwent a successful 13-hour surgery in Egypt. The underdeveloped conjoined twin, Islaam, was attached ...
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.
The Clayton County Police Department said an investigation into the childbirth death at Southern Regional Medical Center is now underway
Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, affecting the first branchial (or pharyngeal) arch, the precursor of the maxilla and mandible.