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AU10034 LCL from B-Lymphocyte

Description:

AUTISTIC DISORDER

Affected:

No Data

Sex:

Male

Age:

2 YR (At Sampling)

  • Overview
  • Phenotypic Data
  • External Links
  • Culture Protocols

Overview

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Repository Autism
Class Disorders of Uncertain Biochemical Etiology
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source LCL from B-Lymphocyte
Race Caucasian
Family Member 2
Relation to Proband brother
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Multiple congenital anomalies; macrocephaly; hypotonia; mild pulmonic stenosis; multicystic right kidney removed; negative MRI; 46,XY; negative for fragile X

Phenotypic Data

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Demographic Data
Relation to Proband brother
Age at Sampling 2 YR
Sex Male
Age of Onset(If not a control) No Data
Age at Diagnosis(If not a control) No Data
Hispanic or Latino/Not Hispanic or Latino not yet reported
Racial Category Caucasian
Country No Data
Diagnosed By No Data
 
Data Elements
Clinical Element Type: Autism
  (Baseline)
DSM-IV Criteria
Qualitative Impairment in Social Interaction as Manifested by at Least Two of the Following Eye-to-eye gaze
Facial expression
Body postures
Body gestures
Failure to develop peer relationships appropriate to developmental levels
Lack of spontaneous seeking to share enjoyment or achievements with other people
Lack of social or emotional reciprocity
Qualitative Impairment in Communication Delay in, or total lack of, the development of spoken language (not accompanied by an attempt to compensate through alternative modes of communcation such as gesture or mime)
Delay in individuals with adequate speech, marked impairment in the ability to initiate or sustain a conversation with others
Stereotyped and repetitive use of language or idiosyncratic language
Lack of varied, spontaneous make-believe play or social initiative play appropriate to developmental level
Restricted, Repetitive, and Stereotypes, Patterns of Behavior, Interests and Activities as Manifested by at Least One of the Following Encompassing preoccupation with one or more stereotyped and restricted patterns of interest that is abnormal either in intensity or focus
Apparently inflexible adherence to specific, nonfunctional routines or rituals
Stereotyped and repetitive motor mannerisms
Persistent preoocupation with parts or objects
Delays or Abnormal Functioning in at Least One of the Following Areas with Onset Prior to Age 3 Years Social interaction
Language as used in social communication
Symbolic or imaginative play
The disturbance is not better accounted for by Rett Syndrome or Childhood Disintegrative Disorder  No Data
Autism Diagnostic Interview
Qualitative Impairment in Reciprocal Social Interaction  6
Communication - Nonverbal  2
Repetitive Behaviors and Stereotyped Patterns  1
Abnormality of Development Evident at or Before 36 months  3
Autism Diagnostic Observation Schedules
Communication  3
Qualitative Impairment in Reciprocal Social Interaction  3
Communication and Social  6
Play  3
Stereotyped Behaviors and Restricted Interests  0
Background History
Birth Weight  8 LBS 9 OZ
Apagar Score (at 1min;at 5min)  No Data
Maternal Age at Delivery  26 YEARS
Perinatal  GRAVIDA 1; PARA 0. NO DIFFICULTIES WITH PREGNANCY. BORN FULL TERM VIA CAESARIAN SECTION DUE TO CHILD DIAGNOSED VIA ULTRASOUND WITH A RIGHT MULTICYSTIC KIDNEY. CHILD WAS HOSPITALIZED FOR TEN DAYS SECONDARY TO EATING DIFFICULTY.
Developmental  SAT ALONE 9 MONTHS, WALKED INDEPENDENTLY AT 19 MONTHS. LANGUAGE MILESTONES: SAID "MAMA/DADA" AT 18 MONTHS, DOES NOT YET SPEAK IN 2 OR 3 WORD SENTENCES. NO HISTORY OF LANGUAGE REGRESSION.
Health  DIAGNOSED IN UTERO WITH RIGHT MULTICYSTIC KIDNEY. AS AN INFANT UNDERWENT RIGHT NEPHRECTOMY. HAD TWO SURGICAL PROCEDURES FOR SMALL BOWEL OBSTRUCTION. HAD LACRIMAL DUCT STENOSIS REPAIED AT AGE 18 MOTNHS. HAS MILD PULMONIC STENOSIS.
Family/Social  AS REPORTED BY PARENTAL INTERVIEW, MOTHER HAS A HISTORY OF MULIPLE SCLEROSIS AND THE PATERNAL GRANDFATHER HAS LEUKEMIA. BROTHER HAS AUTISTIC DISORDER.
General/Physical Examination
Height (Percentile)  94 CM (50-75%)
Weight (Percentile)  15 KG (90%)
Head Circumference (Percentile)  55 CM (>95%)
Dysmorphic Features  MACROCEPHALY WITH SOME HEAD ASYMMETRY, EARS NORMALLY SHAPED WITH SLIGHT POSTERIOR ROTATION, HIGH ARCHED PALATE
Neurocutaneous Stigmata  NONE
Wood's Lamp Exam positive  negative  
Neurological Examination
Muscle tone  LOW
Muscle strength normal   abnormal 
Deep tendon reflexes symmetric and physiologic  
Plantar response normal  downgoing  
Gait  NO ATAXIA
Involuntary movements present  absent  
Tests/Evaluations
Fragile X positive  negative   unknown 
EEG normal  abnormal  unknown  
CT normal  abnormal  unknown  
Audiologic exam normal  abnormal  unknown  
MRI  NORMAL
Peabody Picture Vocabulary Test (Form IIIB)  STANDARDIZED SCORE - 88
Gessell  N/A
Kaufman Brief Intelligence Test  N/A
WISC III  No Data
RPM  No Data
Metabolic Studies  No Data
Vineland Adaptive Schedules  No Data
Binet  No Data
Stanford-Binet Intelligence Scale  No Data
Slosson Intelligence Scale  No Data
Raven Progressive Matrices  No Data
Bayley Scales of Development  No Data
Developmental Profile II Ability Equivalence  No Data
Remarks Multiple congenital anomalies; macrocephaly; hypotonia; mild pulmonic stenosis; multicystic right kidney removed; negative MRI; 46,XY; negative for fragile X

External Links

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NCBI Gene Gene ID:8311
NCBI GTR 209850 AUTISM
OMIM 209850 AUTISM
Omim Description AUTISM, INFANTILE
  AUTISTIC DISORDER

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
Commercial:
$195.00USD
Academic &
Non-profit:
$195.00USD
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