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Longer titles found: Bilateral frontoparietal polymicrogyria (view)

searching for Polymicrogyria 21 found (70 total)

Setleis syndrome (234 words) [view diff] exact match in snippet view article find links to article

syndrome; a syndrome of focal dermal hypoplasia, morning glory anomaly, and polymicrogyria; incontinentia pigmenti; oculocerebrocutaneous syndrome; Rothmund–Thomson

GPR56 (3,019 words) [view diff] exact match in snippet view article find links to article

cause a severe cortical malformation known as bilateral frontoparietal polymicrogyria (BFPP). Investigating the pathological mechanism of disease-associated

Congenital bilateral perisylvian syndrome (307 words) [view diff] exact match in snippet view article find links to article

surface of the brain. This condition is called bilateral perisylvian polymicrogyria. The sulci, deep grooves on the brain, may also not form correctly.

Cyclin D2 (1,332 words) [view diff] exact match in snippet view article find links to article

testicular tumors. Mutations in CCND2 are associated to megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome. GRCh38: Ensembl release 89: ENSG00000118971

Waney Squier (1,322 words) [view diff] exact match in snippet view article find links to article

peer-reviewed publications ranging in topic from fetal to childhood infection, polymicrogyria, hydrocephalus, head trauma and mimics of trauma caused by vascular

Goldberg–Shprintzen syndrome (1,327 words) [view diff] exact match in snippet view article find links to article

Goldberg–Shprintzen syndrome, as it is much more likely to occur. In particular, polymicrogyria, microcephaly, and hypoplastic corpus callosum have been suggested as

Micropolygyria (160 words) [view diff] exact match in snippet view article find links to article

Micropolygyria Other names Polymicrogyria, Polygyria, or Microgyria Specialty Neurology

AHI1 (1,237 words) [view diff] exact match in snippet view article find links to article

AHI1 Gene, Encoding Jouberin, Cause Joubert Syndrome with Cortical Polymicrogyria". American Journal of Human Genetics. 75 (6): 979–987. doi:10.1086/425985

Perisylvian syndrome (74 words) [view diff] exact match in snippet view article find links to article

Perisylvian syndrome Other names Bilateral perisylvian polymicrogyria Lateral sulcus (Sylvian fissure) Specialty Neurology

Focal dermal hypoplasia (646 words) [view diff] exact match in snippet view article find links to article

to TWIST2 gene mutations. It associated with morning glory anomaly, polymicrogyria, incontinentia pigmenti, oculocerebrocutaneous syndrome, Rothmund-Thomson

Occludin (2,896 words) [view diff] exact match in snippet view article find links to article

thought to be a cause of band-like calcification with simple gyration and polymicrogyria (BLC-PMG). BLC-PMG is an autosomal recessive neurologic disorder. Occludin

Eomesodermin (1,910 words) [view diff] exact match in snippet view article find links to article

silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis". Nature Genetics. 39 (4): 454–6. doi:10

WAGR syndrome (967 words) [view diff] exact match in snippet view article find links to article

Hanson I, Shorvon S, Moore A, van Heyningen V, Sisodiya S (2003). "Polymicrogyria and absence of pineal gland due to PAX6 mutation". Ann Neurol. 53 (5):

Bobby Schuller (523 words) [view diff] exact match in snippet view article find links to article

children. Schuller's son Cohen has a chronic rare brain disease called polymicrogyria which causes epilepsy and intellectual delay. Crystal Cathedral Ministries

Stanislas Lyonnet (884 words) [view diff] exact match in snippet view article find links to article

silencing of T-box transcription factor EOMES leads to microcephaly with polymicrogyria and corpus callosum agenesis. Nat Genet. 2007 Apr;39(4):454-6. Thomas

Aicardi–Goutières syndrome (3,342 words) [view diff] exact match in snippet view article find links to article

occludin cause band-like calcification with simplified gyration and polymicrogyria". The American Journal of Human Genetics. 87 (3): 354–364. doi:10.1016/j

Non-homologous end-joining factor 1 (1,652 words) [view diff] exact match in snippet view article find links to article

Dobyns WB, Villard L (Apr 2007). "Truncation of NHEJ1 in a patient with polymicrogyria". Human Mutation. 28 (4): 356–64. doi:10.1002/humu.20450. PMID 17191205

Congenital mirror movement disorder (2,817 words) [view diff] exact match in snippet view article find links to article

Congenital hemiplegia Moebius syndrome Seckel syndrome Wildervanck syndrome Polymicrogyria The specific molecular mechanism that underpins this movement disorder

Neonatal seizure (4,791 words) [view diff] exact match in snippet view article find links to article

needed] Congenital central nervous system malformations: lissencephaly, polymicrogyria, and tuberous sclerosis are specific entities known to cause seizures

Muscle–eye–brain disease (3,538 words) [view diff] exact match in snippet view article find links to article

cortex Diffused dysplasia Diffused cobblestone lissencephaly Frontal polymicrogyria White matter Uneven T1 and T2 prolongation No myelin in cerebrum or

List of OMIM disorder codes (18,877 words) [view diff] exact match in snippet view article find links to article

epilepsy; 611087; STRADA Polymicrogyria with optic nerve hypoplasia; 613180; TUBA8 Polymicrogyria, asymmetric; 610031; TUBB2B Polymicrogyria, bilateral frontoparietal;