Hydranencephaly

Jump to navigation Jump to search

Template:DiseaseDisorder infobox

WikiDoc Resources for Hydranencephaly

Articles

Most recent articles on Hydranencephaly

Most cited articles on Hydranencephaly

Review articles on Hydranencephaly

Articles on Hydranencephaly in N Eng J Med, Lancet, BMJ

Media

Powerpoint slides on Hydranencephaly

Images of Hydranencephaly

Photos of Hydranencephaly

Podcasts & MP3s on Hydranencephaly

Videos on Hydranencephaly

Evidence Based Medicine

Cochrane Collaboration on Hydranencephaly

Bandolier on Hydranencephaly

TRIP on Hydranencephaly

Clinical Trials

Ongoing Trials on Hydranencephaly at Clinical Trials.gov

Trial results on Hydranencephaly

Clinical Trials on Hydranencephaly at Google

Guidelines / Policies / Govt

US National Guidelines Clearinghouse on Hydranencephaly

NICE Guidance on Hydranencephaly

NHS PRODIGY Guidance

FDA on Hydranencephaly

CDC on Hydranencephaly

Books

Books on Hydranencephaly

News

Hydranencephaly in the news

Be alerted to news on Hydranencephaly

News trends on Hydranencephaly

Commentary

Blogs on Hydranencephaly

Definitions

Definitions of Hydranencephaly

Patient Resources / Community

Patient resources on Hydranencephaly

Discussion groups on Hydranencephaly

Patient Handouts on Hydranencephaly

Directions to Hospitals Treating Hydranencephaly

Risk calculators and risk factors for Hydranencephaly

Healthcare Provider Resources

Symptoms of Hydranencephaly

Causes & Risk Factors for Hydranencephaly

Diagnostic studies for Hydranencephaly

Treatment of Hydranencephaly

Continuing Medical Education (CME)

CME Programs on Hydranencephaly

International

Hydranencephaly en Espanol

Hydranencephaly en Francais

Business

Hydranencephaly in the Marketplace

Patents on Hydranencephaly

Experimental / Informatics

List of terms related to Hydranencephaly


Overview

Hydranencephaly is a type of cephalic disorder. This is a rare condition in which the cerebral hemispheres are absent and replaced by sacs filled with cerebrospinal fluid.

In "hemihydranencephaly", only half of the brain is filled with fluid.[1]

Presentation

Usually the cerebellum and brainstem are formed normally. An infant with hydranencephaly may appear normal at birth. The infant's head size and spontaneous reflexes such as sucking, swallowing, crying, and moving the arms and legs may all seem normal. However, after a few weeks the infant usually becomes irritable and has increased muscle tone (hypertonia). After several months of life, seizures and hydrocephalus may develop. Other symptoms may include visual impairment, lack of growth, deafness, blindness, spastic quadriparesis (paralysis), and intellectual deficits.

Some infants may have additional abnormalities at birth including seizures, myoclonus (involuntary sudden, rapid jerks), and respiratory problems.

Causes

Hydranencephaly is an extreme form of porencephaly, which is characterized by a cyst or cavity in the cerebral hemispheres, and may be caused by vascular insult or injuries, infections, or traumatic disorders after the 12th week of pregnancy.

Diagnosis

Diagnosis may be delayed for several months because the infant's early behavior appears to be relatively normal. Transillumination, an examination in which light is passed through body tissues, usually confirms the diagnosis.

Prognosis

There is no standard treatment for hydranencephaly. Treatment is symptomatic and supportive. Hydrocephalus may be treated with a shunt.

The prognosis for children with Hydranencephaly is generally quite poor. Death usually occurs in the first year of life.[2]

In a survey completed by 88 families of children with Hydranencephaly from 2006-2007, 69% of the children who had died, did so after their first birthday.[citation needed] The oldest of the children who had died was in their 20s. 62% of the children represented in the survey were over the age of 1 at the time it was filled out. The first year is the hardest for children with Hydranencephaly but survival is possible.

In 2003, the oldest known survivor was 20 1/2 years old.[3]

Noncortical responses to auditory stimuli have been observed in some patients.[4]

References

  1. Ulmer S, Moeller F, Brockmann MA, Kuhtz-Buschbeck JP, Stephani U, Jansen O (2005). "Living a normal life with the nondominant hemisphere: magnetic resonance imaging findings and clinical outcome for a patient with left-hemispheric hydranencephaly". Pediatrics. 116 (1): 242–5. doi:10.1542/peds.2004-0425. PMID 15995064.
  2. McAbee GN, Chan A, Erde EL (2000). "Prolonged survival with hydranencephaly: report of two patients and literature review". Pediatr. Neurol. 23 (1): 80–4. PMID 10963978.
  3. Covington C, Taylor H, Gill C; et al. (2003). "Prolonged survival in hydranencephaly: a case report". Tennessee medicine : journal of the Tennessee Medical Association. 96 (9): 423–4. PMID 14513530.
  4. Counter SA (2007). "Preservation of brainstem neurophysiological function in hydranencephaly". doi:10.1016/j.jns.2007.06.043. PMID 17719607.

External links

Template:Congenital malformations and deformations of nervous system Template:WH Template:WikiDoc Sources