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  2. Cephalic disorder - Wikipedia

    en.wikipedia.org/wiki/Cephalic_disorder

    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 ...

  3. Microcephaly - Wikipedia

    en.wikipedia.org/wiki/Microcephaly

    There are a variety of symptoms that can occur in children. Infants with microcephaly are born with either a normal or reduced head size. [10] Subsequently, the head fails to grow, while the face continues to develop at a normal rate, producing a child with a small head and a receding forehead, and a loose, often wrinkled scalp. [11]

  4. Scaphocephaly - Wikipedia

    en.wikipedia.org/wiki/Scaphocephaly

    Scaphocephaly or sagittal craniosynostosis is a type of cephalic disorder which occurs when there is a premature fusion of the sagittal suture. Premature closure results in limited lateral expansion of the skull, resulting in a characteristic long, narrow head. [1] The skull base is typically spared. [2]

  5. Macrocephaly-capillary malformation - Wikipedia

    en.wikipedia.org/wiki/Macrocephaly-capillary...

    Some children are born with structural brain anomalies such as cortical dysplasia or polymicrogyria. While developmental delay is nearly universal in this syndrome it is variable in severity, with the majority having mild to moderate delays and a minority having severe cognitive impairment. Some patients are affected with a seizure disorder.

  6. Category:Congenital disorders of nervous system - Wikipedia

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

    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-Q07 within Chapter XVII: Congenital malformations, deformations and chromosomal abnormalities should be included in this category.

  7. Colpocephaly - Wikipedia

    en.wikipedia.org/wiki/Colpocephaly

    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 ...

  8. Macrocephaly - Wikipedia

    en.wikipedia.org/wiki/Macrocephaly

    Macrocephaly is a condition in which circumference of the human head is abnormally large. [1] It may be pathological or harmless, and can be a familial genetic characteristic. . People diagnosed with macrocephaly will receive further medical tests to determine whether the syndrome is accompanied by particular disorde

  9. Porencephaly - Wikipedia

    en.wikipedia.org/wiki/Porencephaly

    Porencephaly is an extremely rare cephalic disorder involving encephalomalacia. [1] It is a neurological disorder of the central nervous system characterized by cysts or cavities within the cerebral hemisphere. [2] Porencephaly was termed by Heschl in 1859 to describe a cavity in the human brain. [3]