Acephaly (medicine)
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(Redirected from Acephaly)
| Acephaly (medicine) Classification and external resources | |
| ICD-10 | Q00.0 |
|---|---|
For "acephaly" as a poetic device, see Acephalous line.
Acephaly is a type of cephalic disorder. This literally means absence of the head. It is a much rarer condition than anencephaly. The acephalic fetus is a parasitic twin attached to an otherwise intact fetus. The acephalic fetus has a body but lacks a head and heart; the fetus's neck is attached to the normal twin. The blood circulation of the acephalic fetus is provided by the heart of the twin. The acephalic fetus can not exist independently of the fetus to which it is attached. Similarly, acardiac fetuses lack everything from the heart upwards, including head and arms, and behave similarly to acephalic fetuses.
External links
Congenital malformations and deformations of nervous system (Q00-Q07, 740-742) | |
|---|---|
| Brain | Anencephaly (Acephaly, Acrania, Iniencephaly) - Encephalocele - Microcephaly - Congenital hydrocephalus (Dandy-Walker syndrome) - other reduction deformities (Holoprosencephaly, Lissencephaly, Pachygyria, Hydranencephaly) - Septo-optic dysplasia - Megalencephaly - Congenital cerebral cysts (Porencephaly, Schizencephaly) - Congenital brain tumors |
| Brain stem | Arnold-Chiari malformation |
| Spinal cord | Spina bifida - Currarino syndrome - Sacrococcygeal teratoma - Diastematomyelia - Syringomyelia |
| see also non-congenital CNS and PNS (G, 320-359) | |
