| Demographic Data |
| Relation to Proband |
proband |
| Age at Sampling |
2 YR |
| Sex |
Female |
| Age at Diagnosis(If not a control) |
3 DA |
| 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 |
yes no unknown |
| Was child breast-fed? |
yes no unknown |
| If yes, duration in months |
2 DAYS |
| Failure to thrive? |
yes no unknown |
| Molecular/Enzyme Laboratory Test Results |
| Which Gene: PCCA? |
yes no unknown |
| Which Gene: PCCB? |
No Data |
| Mutations Allele 1 |
K298R |
| Mutations Allele 2 |
DEL EX 13-20 |
| Family History |
| Are there other family members with PA? |
yes no unknown |
| Other affected relatives? |
yes no unknown |
| Has the individual passed away? |
No Data |
| Clinical Evaluation |
| Current weight in kgs |
15 |
| Current height in cms |
91 |
| Respiratory |
| Apnea |
yes no unknown |
| Tachypnea |
yes no unknown |
| Cardiovascular |
| Cardiomyopathy |
yes no unknown |
| Long QT? |
yes no unknown |
| If yes, type |
No Data |
| Abdominal/Gastrointestinal |
| Pancreatitis |
chronic acute never noted |
| Kidney problems |
yes no unknown |
| Liver transplant |
yes no unknown |
| Port-a-cath |
currently in place not currently in place never had one |
| Gut motility |
normal slow requires medication unknown |
| Reflux |
yes no unknown |
| List medications |
PREVACID |
| Eating by mouth |
0% |
| Tube fed |
yes no unknown |
| If yes, what kind |
GJ-tube |
| Vomiting |
once a month or more |
| Are anti-emetics used for vomiting |
yes no unknown |
| Neurologic |
| Basal ganglia damage |
yes no unknown |
| If yes, determined by |
No Data |
| Seizures |
yes no unknown |
| Autism spectrum disorder |
yes no unknown |
| ADD/ADHD |
yes no unknown |
| Optic nerve damage |
yes no unknown |
| Neutropenia |
chronic acute unknown |
| Anemia |
yes no unknown |
| 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 |
| 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 |
age appropriate |
| Age when first talked |
1 YEAR |
| Congitive ability |
mildly impaired |
| IQ |
known untested unsure |
| Metabolic |
| Is the individual biotin responsive |
yes no unknown |
| Episodes of ketoacidosis |
yes no unknown |
| Chronic hyperammonemia |
yes no unknown |
| Is the individual currently on metabolic formula |
yes no unknown |
| If yes, which ones |
Propimex
Polcyose
|
| Is the individual taking levocarnitine |
yes no unknown |
| Other supllements |
Biotin
Iron
|
| Remarks |
Clinically affected; diagnosed at 3 days of age by newborn screening; failure to thrive; no family history; mitral valve regurgitation; normal gut motility; reflux; no eating by mouth; GJ-tube; vomiting once a month or more; acute neutropenia; chronic anemia; acute low platelets; walked at 16 months of age; talked at age 1 year; mildly impaired cognitive ability; on metabolic formula and levocarnitine; donor subject is a compound heterozygote: allele 1: has a substitution of arginine for lysine at codon 298 in exon 11 of the PCCA gene [Lys298Arg (K298R)] and allele 2: has a deletion of exons 13-20 |