• Thumbnail for Schizencephaly
    and psychomotor retardation. Schizencephaly can be distinguished from porencephaly by the fact that in schizencephaly, the fluid-filled component is...
    9 KB (825 words) - 04:52, 27 July 2024
  • Thumbnail for Septo-optic dysplasia
    neurological abnormalities such as cortical dysplasia, polymicrogyria and schizencephaly. Such abnormalities are always identified when spastic quadriplegia...
    11 KB (1,077 words) - 07:23, 15 April 2024
  • Robinow syndrome Rubinstein–Taybi syndrome Saethre–Chotzen syndrome Schizencephaly Scoliosis Sickle cell disease Sirenomelia Situs inversus Smith–Lemli–Opitz...
    4 KB (357 words) - 13:01, 28 September 2024
  • (2012). Cingulate cortex aplasia and callosal dysgenesia combined with schizencephaly in a patient with chronic lying. General Hospital Psychiatry, 34(3)...
    21 KB (2,426 words) - 02:07, 29 September 2024
  • (Q04.3) Megalencephaly (Q04.5) Microcephaly (Q02) Porencephaly (Q04.6) Schizencephaly (Q04.6) Acephaly (Q00.0) Exencephaly (Q00.0) Macrocephaly (Q75.3) Micrencephaly...
    5 KB (503 words) - 19:01, 26 May 2024
  • Thumbnail for Cerebral cortex
    of genetic disorders of the cerebral cortex, including microcephaly, schizencephaly and types of lissencephaly. Chromosome abnormalities can also result...
    69 KB (8,050 words) - 23:04, 8 November 2024
  • Thumbnail for Colpocephaly
    Periventricular leukomalacia (PVL) intraventricular hemorrhage Hydrocephalus schizencephaly microgyria microcephaly Pierre-Robin syndrome Neurofibromatosis Often...
    17 KB (2,052 words) - 13:30, 25 July 2024
  • disease Sanfilippo syndrome Schilder's disease (two distinct conditions) Schizencephaly Sclerosis Seizures Sensory processing disorder Septo-optic dysplasia...
    13 KB (1,143 words) - 03:22, 23 October 2024
  • Hydrocephalus Neuronal migration disorders such as grey matter heterotopia Schizencephaly Agenesis of the corpus callosum is caused by disruption to development...
    10 KB (925 words) - 06:02, 7 July 2024
  • prevention for developmental brain disorders such as porencephaly. Schizencephaly Gul A, Gungorduk K, Yildirim G, Gedikbasi A, Ceylan Y (2009). "Prenatal...
    18 KB (2,157 words) - 19:20, 2 July 2024
  • Schinzel–Giedion midface retraction syndrome Schisis association Schistosomiasis Schizencephaly Schizoaffective disorder Schizoid personality disorder Schizophrenia...
    23 KB (1,933 words) - 06:25, 11 July 2024
  • Thumbnail for Neural tube defect
    include anencephaly, encephaloceles, hydranencephaly, iniencephaly, schizencephaly, and the most common form, spina bifida. Closed NTDs occur when the...
    50 KB (5,814 words) - 12:37, 7 June 2024
  • development of the septum pellucidum, malformations of the pituitary gland, schizencephaly, cortical heterotopia, white matter hypoplasia, pachygyria, and holoprosencephaly...
    18 KB (2,204 words) - 01:43, 29 July 2024
  • Kidney (purple, teal & green), Pseudotumor Cerebri (green & blue), Schizencephaly (green & purple), Sticklers Syndrome (green & purple), Thyroid Cancer...
    18 KB (1,667 words) - 22:18, 21 June 2024
  • Thumbnail for Hydranencephaly
    Hydranencephaly is sometimes misdiagnosed as bilaterally symmetric schizencephaly (a less destructive developmental process on the brain), severe hydrocephalus...
    11 KB (1,076 words) - 19:41, 3 October 2024
  • Thumbnail for EMX2
    EMX2 is negatively regulated by HOXA10. EMX2 has been associated with Schizencephaly, a disease where there are large parts of the brain hemispheres absent...
    8 KB (948 words) - 22:33, 29 January 2023
  • perinatal brain injury, lead encephalopathy, hydrocephalus, prosencephaly, schizencephaly, and other diagnoses. It was originally the Hunterdon State School and...
    3 KB (292 words) - 22:51, 25 August 2024
  • mutations in the COL4A1 gene occur in some patients with porencephaly and schizencephaly. In humans, a novel mutation of the COL4A1 gene coding for collagen...
    21 KB (2,425 words) - 14:05, 9 October 2024
  • Thumbnail for Dandy–Walker malformation
    lissencephaly (shallower ridges), polymicrogyria, holoprosencephaly and schizencephaly. Individuals with these features tend to have developmental delay or...
    47 KB (5,483 words) - 15:13, 2 March 2024
  • neurocutaneous syndromes and epilepsy, neuronal substrates and epilepsy, schizencephaly, arhinencephalia, mental retardation, decussation of the bulbar pyramidal...
    7 KB (715 words) - 18:32, 1 March 2024
  • Thumbnail for Neuronal migration disorder
    differs greatly between syndromes. Lissencephaly Microlissencephaly Schizencephaly Porencephaly Pachygyria Polymicrogyria Agyria Macrogyria Microgyria...
    7 KB (690 words) - 13:11, 25 July 2024
  • "A unitary model of schizophrenia: Bleuler's "fragmented phrene" as schizencephaly". Archives of General Psychiatry. 56 (9): 781–7. doi:10.1001/archpsyc...
    75 KB (8,519 words) - 05:34, 2 November 2024
  • Thumbnail for Collagen, type IV, alpha 1
    mutations in the COL4A1 gene occur in some patients with porencephaly and schizencephaly. In humans, a novel mutation of the COL4A1 gene coding for collagen...
    19 KB (2,484 words) - 16:19, 1 July 2024
  • Thumbnail for Foix–Chavany–Marie syndrome
    XII (the hypoglossal nerve). Cerebral malformation, namely unilateral schizencephaly in association with contralateral polymicrogyria symmetrically in the...
    22 KB (2,582 words) - 00:22, 5 February 2024
  • "A unitary model of schizophrenia: Bleuler's "fragmented phrene" as schizencephaly". Archives of General Psychiatry. 56 (9): 781–7. doi:10.1001/archpsyc...
    53 KB (5,478 words) - 11:41, 19 November 2024
  • Thumbnail for HESX1
    (2010). "Candidate gene sequencing of LHX2, HESX1, and SOX2 in a large schizencephaly cohort". Am. J. Med. Genet. A. 152A (11): 2736–42. doi:10.1002/ajmg...
    8 KB (1,024 words) - 01:12, 3 October 2024
  • 609241; NAGA Schinzel–Giedion midface retraction syndrome; 269150; SETBP1 Schizencephaly; 269160; EMX2 Schizophrenia; 181500; DISC2 Schneckenbecken dysplasia;...
    234 KB (18,877 words) - 06:16, 6 November 2024
  • Transcriptional regulator for cell differentiation; sequence-specific DNA binding Schizencephaly Two-hybrid screen Proline Rich 20D (PRR20D) Unknown function Pull down...
    22 KB (1,795 words) - 20:14, 20 September 2023