Disease #04217 (WEST (West syndrome (WEST, epileptic encephalopathy, early infantile)))

Official abbreviation WEST
Name West syndrome (WEST, epileptic encephalopathy, early infantile)
OMIM ID -
Inheritance -
Individuals reported having this disease 7
Phenotype entries for this disease 6
Associated with 0 genes -
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Date created 2015-03-06 11:05:39 +01:00 (CET)
Date last edited N/A


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00033729 - - patient affceted with West Syndrome M yes Algeria - - - - - WEST - GUF1 GUF1 1 5 Alexandre Reymond
00229582 Fam3 - - M no Australia - - - - - WEST Severe neonatal onset epileptic encephalopathy. ARX ARX 1 1 Marie Shaw
00317979 Fam1Pat1 PubMed: Hamada 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M no Japan - - - - - WEST see paper; ... PHACTR1 PHACTR1, PSG6, SCNN1D, STARD9, THEG, TNXB, TTLL5 10 1 Johan den Dunnen
00317980 Fam2Pat2 PubMed: Hamada 2018 2-generation family, 1 affected, unaffected heterozygous carrier parents M - Japan - - - - - WEST see paper; ... PHACTR1 PHACTR1 1 1 Johan den Dunnen
00359659 patient PubMed: Pena-Padilla 2021 - M - Mexico - - - - - WEST see paper; ... DMD DMD 1 1 Johan den Dunnen
00391760 3.II:3 PubMed: DiScipio 2020 - M - - - - - - - WEST Nystagmus - infancy, Photophobia - infancy, visual acuity right/left eye: 20/200: 20/250, Contrast Sensitivity: 0.75:0.75, , Color vision: Strong RG & moderate BY deficit, Refractive error -8.50/+1.25 × 115: -8.00/+1.00 × 70, Retinal exam: Tilted disc; dull foveal reflex; peripheral lattice; Fundus autofluorescence: subtle foveal hyper-AF, Grade 1 foveal hypoplasia; Optical Coherence Tomography: Mild disruption of outer segments, in central, sub-foveal regi CNGB3 CNGB3 2 1 LOVD
00395953 patient PubMed: Razaq 2021 - M no United States Middle East;Hispanic - - - - BMD/DMD, WEST 4m-epileptic spasms, no head control; 5m-EEG hypsarrhythmia; 9m-severe developmental delay; MRI brain cortical atrophy; 18m-raised CK 25,000, 20m- DMD DMD, G6PC, PAH, RARS2 4 1 Johan den Dunnen
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