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 |