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Chiari malformation or Arnold–Chiari malformation should not be confused with Budd–Chiari syndrome, [53] a hepatic condition also named for Hans Chiari. In Pseudo-Chiari Malformation, leaking of CSF may cause displacement of the cerebellar tonsils and similar symptoms sufficient to be mistaken for a Chiari I malformation.
Many organ systems are affected by triploidy, but the central nervous system and skeleton are the most severely affected: . Common central nervous system defects seen in triploidy include holoprosencephaly, hydrocephalus (increased amount of cerebrospinal fluid within the brain), ventriculomegaly, Arnold–Chiari malformation, agenesis of the corpus callosum and neural tube defects.
Arnold–Chiari malformation, or simply "Chiari malformation", a malformation of the brain; Budd–Chiari syndrome, a disease with typical symptoms of abdominal pain, ascites and hepatomegaly caused by occlusion of the hepatic veins; Chiari–Frommel syndrome, an older term for hyperprolactinaemia with extended postpartum galactorrhea and ...
Spinal compression and the resulting relief is a known issue with this disorder. Like with the early-onset form, this disease form is linked to the Arnold–Chiari malformation, in which the brain is pulled or lowers into the top of the spine. [29]
Fetal surgery in utero before 26 weeks gestation has been performed with some hope that there is benefit to the outcome including a reduction in Arnold–Chiari malformation and thereby decreases the need for a ventriculoperitoneal shunt but the procedure is very high risk for both mother and baby and is considered extremely invasive with ...
Arnold was the author of 120 articles in the fields of histology and pathological anatomy. [ 1 ] With Austrian pathologist, Hans Chiari , his name is lent to a condition known as Arnold–Chiari malformation , a disorder that takes place when the cerebellar tonsils and the medulla oblongata protrude through the foramen magnum into the spinal ...
Budd–Chiari syndrome is a condition when an occlusion or obstruction in the hepatic veins prevent normal outflow of blood from the liver. The symptoms are non-specific and vary widely, but it may present with the classical triad of abdominal pain, ascites, and liver enlargement. Untreated Budd-Chiari syndrome can result in liver failure. [1]
Arnold–Chiari malformation; B. Bannayan–Zonana syndrome; Bardet–Biedl syndrome; Barth syndrome; Basal-cell nevus syndrome; Beckwith–Wiedemann syndrome;
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