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NA22083 DNA from LCL

Description:

PROPIONIC ACIDEMIA

Affected:

Yes

Sex:

Male

Age:

4 YR (At Sampling)

  • Overview
  • Characterizations
  • Phenotypic Data
  • External Links

Overview

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Repository NIGMS Human Genetic Cell Repository
Subcollection Heritable Diseases
Quantity 25 µg
Quantitation Method Please see our FAQ
Biopsy Source Peripheral vein
Cell Type B-Lymphocyte
Tissue Type Blood
Transformant Epstein-Barr Virus
Sample Source DNA from LCL
Race White
Relation to Proband proband
Confirmation Clinical summary/Case history
Species Homo sapiens
Common Name Human
Remarks Clinically affected; diagnosed at 3 weeks of age; failure to thrive; no family history as far as the adoptive parents know; acute pancreatitis; port-a-cath currently in place; normal gut motility; gastroesophageal reflux; eating by mouth less than 50% of the time; gastric tube; vomiting once a week or more; MRI shows basal ganglia damage; autism spectrum disorder; acute neutropenia; walked at 16 months of age; language is significantly below age level; talked at 20-21 months of age; cognitive ability moderately impaired; infrequent episodes of ketoacidosis; on metabolic formula and levocarnitine

Characterizations

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

Phenotypic Data

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Demographic Data
Relation to Proband proband
Age at Sampling 4 YR
Sex Male
Racial Category White
 
Data Elements
Clinical Element Type: Propionic Acidemia
  (Baseline)
Neonatal Data
Was this child newborn screened? yes  no   unknown 
If yes, was the result prior to hospitalization  No Data
Weight at birth in kgs  2.7
Length at birth in cm  48.2
Was child breast-fed? yes  no   unknown 
If yes, duration in months  No Data
Failure to thrive? yes   no  unknown 
Molecular/Enzyme Laboratory Test Results
Which Gene: PCCA? yes  no  unknown  
Which Gene: PCCB? yes  no  unknown  
Mutations Allele 1  No Data
Mutations Allele 2  No Data
Method (if known)  No Data
Enzyme activity - % of normal  No Data
Absolute amount  No Data
Family History
Are there other family members with PA? yes  no   unknown 
Number of siblings with PA  ADOPTIVE PARENTS KNOW OF NO AFFECTED SIBS
Number of living siblings with PA  No Data
Other affected relatives? yes  no   unknown 
If so, Relationship  No Data
Has the individual passed away?  No Data
If yes, age at death  No Data
Clinical Evaluation
Current weight in kgs  18.3
Current height in cms  108
Respiratory
Apnea yes  no   unknown 
Tachypnea yes  no   unknown 
Cardiovascular
Cardiomyopathy yes  no   unknown 
If yes, type  No Data
Age at diagnosis of cardiomyopathy  No Data
Age at time of transplant  No Data
Long QT?  No Data
If yes, type  No Data
Age at diagnosis of long QT  No Data
Abdominal/Gastrointestinal
Pancreatitis chronic  acute   never noted 
Kidney problems yes  no   unknown 
Liver transplant yes  no   unknown 
If yes, age at transplant  No Data
Port-a-cath currently in place   not currently in place  never had one 
Gut motility normal   slow  requires medication  unknown 
List medications  No Data
Reflux yes   no  unknown 
List medications  PREVACID
Eating by mouth  1-50%
Tube fed yes   no  unknown 
If yes, what kind  G-tube
Vomiting  once a week or more
Are anti-emetics used for vomiting  No Data
List medications  No Data
Neurologic
Basal ganglia damage yes   no  unknown 
If yes, determined by MRI   CT  Other  unknown 
Seizures yes  no   unknown 
If yes, type and frequency  No Data
Autism spectrum disorder yes   no  unknown 
ADD/ADHD yes  no  unknown  
Optic nerve damage yes  no  unknown  
If yes, age at detection  No Data
Neutropenia chronic  acute   unknown 
List medications  No Data
Anemia  No Data
If yes, type of anemia  No Data
Immune deficiency yes  no   unknown 
Treated with IVIG  No Data
Low platelets chronic  acute  not applicable   unknown 
Asthma yes  no   unknown 
Secondary hip dysplasia yes  no   unknown 
Broken bones yes  no   unknown 
If yes, type of fracture and location  No Data
Short stature yes  no   unknown 
Growth hormone treatment yes  no   unknown 
Osteoporosis yes  no  unknown  
Developmental Evaluation
Walking  100% of the time
Age when first walked  16 MONTHS
Language  significantly below age level
Age when first talked  20-21 MONTHS
Congitive ability  moderately impaired
IQ known  untested  unsure  
If known, give value or age level  No Data
Metabolic
Is the individual biotin responsive yes  no   unknown 
Episodes of ketoacidosis yes   no  unknown 
If yes, give frequency  infrequently
Chronic hyperammonemia  No Data
Currently elevated  No Data
Is the individual currently on metabolic formula yes   no  unknown 
If yes, which ones Propimex
SHS XMTVI
OA
Pro-phree
PFD
80056
Duocal
Polcyose
Vitaflo
Is the individual taking levocarnitine yes   no  unknown 
If yes, mg/kg  200MG/KG
Other supllements Co-Q10
DHA
Vitamin E
B-6
Biotin
Thiamin
Multi-vitamin
Iron
Other
None
Unknown
Remarks Clinically affected; diagnosed at 3 weeks of age; failure to thrive; no family history as far as the adoptive parents know; acute pancreatitis; port-a-cath currently in place; normal gut motility; gastroesophageal reflux; eating by mouth less than 50% of the time; gastric tube; vomiting once a week or more; MRI shows basal ganglia damage; autism spectrum disorder; acute neutropenia; walked at 16 months of age; language is significantly below age level; talked at 20-21 months of age; cognitive ability moderately impaired; infrequent episodes of ketoacidosis; on metabolic formula and levocarnitine

External Links

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GEO GEO Accession No: GSM1050451
GEO Accession No: GSM1050452
NCBI GTR 606054 PROPIONIC ACIDEMIA
OMIM 606054 PROPIONIC ACIDEMIA
Omim Description PROPIONIC ACIDEMIA
Pricing
International/Commercial/For-profit:
$281.00USD
U.S. Academic/Non-profit/Government:
$139.00USD
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