hydranencephaly
MeSH: D006832ORPHA: 2177
Overview
congenital disorder of nervous system
Available Treatments (0)
No treatments linked yet
Clinical trials or compassionate use may be available — consult a specialist.
Clinical Presentation
Signs and symptoms associated with hydranencephaly, sourced from HPO and Orphanet clinical annotations.
BlindnessGlobal developmental delayIntrauterine growth retardationCerebral cortical atrophyInfantile sensorineural hearing impairmentPostnatal growth retardationAbnormal corpus striatum morphologyHypotelorismSeizureLethargySpastic diplegiaMeningitisOpisthotonusDilatation of the ventricular cavityAntenatal intracerebral hemorrhageAbnormal cerebral artery morphologyAbnormal dura mater morphologyAbnormal fontanelle morphologyThalamic edemaDysgenesis of the thalamusStiff neckHypoplastic hippocampusAtrophic pituitary glandAbnormal internal carotid artery morphologyChorioretinal atrophyOptic nerve hypoplasiaVentriculomegalyPrimary microcephaly
Classification & Codes
MeSH Code
D006832Orphanet Code
ORPHA:2177hydranencephaly
| MeSH | D006832 |
| Orphanet | ORPHA:2177 |
| Treatments | 0 drug(s) |
| Symptoms on record | 28 signs |
| Status | published |
Factual Authority
Last Updated3/20/2026
Clinical DataHPO · Orphanet
Drug DataFDA · EMA · CDSCO