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Cephalic disorders (from Greek κεφαλή 'head') are congenital conditions that stem from damage to, or abnormal development of, the budding nervous system.. Cephalic disorders are not necessarily caused by a single factor, but may be influenced by hereditary or genetic conditions, nutritional deficiencies, or by environmental exposures during pregnancy, such as medication taken by the ...
Cebocephaly causes: two separate eyes set close together [1] a small, flat nose with a single nostril [1] ear abnormalities [2] mouth abnormalities (such as microstomia) [1] The presence of a nasal septum precludes a diagnosis of cebocephaly. [3] Cebocephaly may cause malformations of the sphenoid and ethmoid bones behind the orbit. [1]
1 Signs and symptoms. 2 Diagnosis. 3 Causes. ... is a cephalic disorder in which the ... babies are born with normal or near-normal brain development and facial ...
Infants with extensive defects show symptoms of the disorder shortly after birth, and the diagnosis is usually made before the age of 1. [2] [7] The following text lists out common signs and symptoms of porencephaly in affected individuals along with a short description of certain terminologies. [2] [6] [7] [8]
Anencephaly is the absence of a major portion of the brain, skull, and scalp that occurs during embryonic development. [1] It is a cephalic disorder that results from a neural tube defect that occurs when the rostral (head) end of the neural tube fails to close, usually between the 23rd and 26th day following conception. [2]
Colpocephaly is a cephalic disorder involving the disproportionate enlargement of the occipital horns of the lateral ventricles and is usually diagnosed early after birth due to seizures. It is a nonspecific finding and is associated with multiple neurological syndromes , including agenesis of the corpus callosum , Chiari malformation ...
The virus usually causes mild, cold-like symptoms, and most people recover in a week or two. ... Children who have neuromuscular disorders, including those who have difficulty swallowing or ...
This disorder was recognized as a distinct syndrome in 1997 and named macrocephaly-cutis marmorata telangiectasia congenita or M-CMTC. [12] [13] A new name, macrocephaly-capillary malformation, abbreviated M-CM, was recommended in 2007. [14] This new name was chosen to more accurately describe the skin markings associated with this disorder.