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GM20087 LCL from B-Lymphocyte

Description:

ENCEPHALOPATHY OF CHILDHOOD (LENNOX-GASTAUT SYNDROME)
DUPLICATED CHROMOSOME

Affected:

Yes

Sex:

Female

Age:

14 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • Publications
  • External Links
  • Culture Protocols

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Chromosome Abnormalities
dbGaP
Class Disorders of the Nervous System
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Black/African American
Ethnicity AFRICAN-AMERICAN
Relation to Proband proband
Confirmation Karyotypic analysis after cell line submission to CCR
ISCN 46,XX,dup(18)(q12.3q22).ish dup(18)(q12.3q22)(wcp18+).arr 4q31.21q31.22(144975019-145163047)x1,18q12.3q22.1(35775026-61034249)x3
Species Homo sapiens
Common Name Human
Remarks Clinically affected; birth weight 6 pounds 1/4 ounce at term; feeding problems during infancy; mental retardation; seizure disorder developed at age 7 years; stopped taking oral feeds at age 14 years when malrotation was identified; severely delayed developmental milestones: wheelchair bound, nonverbal, can not feed self, totally dependent for toileting needs; excessive drooling; normal pinna; broad, flat forehead; flat malar processes; flexion contractions of the distal interphalangeal joints on the fourth and fifth digits of the left hand and an absent flexion crease of the left distal interphalangeal joint on the fifth finger; flexor tone; two to three beats of clonus noted in lower extremities; tight heel cords bilaterally; flexion contractures of knees and elbows bilaterally; widened reflex zone at knees and hyperactive patellar reflex; exotropia; hyperpigmented macule on chest with irregular borders.

Characterizations

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IDENTIFICATION OF SPECIES OF ORIGIN Species of Origin confirmed by LINE assay
 

Phenotypic Data

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Remarks Clinically affected; birth weight 6 pounds 1/4 ounce at term; feeding problems during infancy; mental retardation; seizure disorder developed at age 7 years; stopped taking oral feeds at age 14 years when malrotation was identified; severely delayed developmental milestones: wheelchair bound, nonverbal, can not feed self, totally dependent for toileting needs; excessive drooling; normal pinna; broad, flat forehead; flat malar processes; flexion contractions of the distal interphalangeal joints on the fourth and fifth digits of the left hand and an absent flexion crease of the left distal interphalangeal joint on the fifth finger; flexor tone; two to three beats of clonus noted in lower extremities; tight heel cords bilaterally; flexion contractures of knees and elbows bilaterally; widened reflex zone at knees and hyperactive patellar reflex; exotropia; hyperpigmented macule on chest with irregular borders.

Publications

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Tang Z, Berlin DS, Toji L, Toruner GA, Beiswanger C, Kulkarni S, Martin CL, Emanuel BS, Christman M, Gerry NP, A dynamic database of microarray-characterized cell lines with various cytogenetic and genomic backgrounds G3 (Bethesda, Md)3:1143-9 2013
PubMed ID: 23665875

External Links

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dbSNP dbSNP ID: 13450
NCBI GTR 606369 MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
OMIM 606369 MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
Omim Description ENCEPHALOPATHY OF CHILDHOOD

Culture Protocols

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Split Ratio 1:5
Temperature 37 C
Percent CO2 5%
Medium Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent
Serum 15% fetal bovine serum Not Inactivated
Substrate None specified
Subcultivation Method dilution - add fresh medium
Supplement -
Pricing
International/Commercial/For-profit:
$373.00USD
U.S. Academic/Non-profit/Government:
$216.00USD
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