Demographic Data |
Relation to Proband |
proband |
Age at Sampling |
5 YR |
Sex |
Female |
Age at Diagnosis(If not a control) |
1 WK |
Hispanic or Latino/Not Hispanic or Latino |
Not Hispanic/Latino |
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 |
Weight at birth in kgs |
2.52 |
Length at birth in cm |
47 |
Was child breast-fed? |
yes no unknown |
Failure to thrive? |
yes no unknown |
Molecular/Enzyme Laboratory Test Results |
Which Gene: PCCA? |
yes no unknown |
Which Gene: PCCB? |
yes no unknown |
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 |
24.7 |
Current height in cms |
106 |
Respiratory |
Apnea |
yes no unknown |
Tachypnea |
yes no unknown |
Cardiovascular |
Cardiomyopathy |
yes no unknown |
Long QT? |
yes no unknown |
If yes, type |
chronic acute |
Age at diagnosis of long QT |
5 YRS |
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 |
List medications |
REGLAN, MIRALAX |
Reflux |
yes no unknown |
List medications |
PREVACID, CARAFATE |
Eating by mouth |
1-50% |
Tube fed |
yes no unknown |
If yes, what kind |
G-tube |
Vomiting |
once a month or more |
Are anti-emetics used for vomiting |
yes no unknown |
List medications |
ZOFRAN |
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 |
List medications |
NEUPOGEN |
Anemia |
yes no unknown |
Immune deficiency |
yes no unknown |
Treated with IVIG |
yes no unknown |
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 |
PROXIMAL RT FIBULA/DISTAL RT RADIUS |
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 |
18 MONTHS |
Language |
slightly below age level |
Age when first talked |
2 YRS |
Congitive ability |
age appropriate |
IQ |
known untested unsure |
Metabolic |
Is the individual biotin responsive |
yes no unknown |
Episodes of ketoacidosis |
yes no unknown |
If yes, give frequency |
once a month or more |
Chronic hyperammonemia |
yes no unknown |
Is the individual currently on metabolic formula |
yes no unknown |
If yes, which ones |
Propimex Pro-phree Polcyose Vitaflo
|
Is the individual taking levocarnitine |
yes no unknown |
If yes, mg/kg |
81 |
Other supllements |
Thiamin
|
Remarks |
Clinically affected; diagnosed at age 1 week by newborn screening; failure to thrive; no family history; apnea; chronic long QT diagnosed at age 5 years; gut motility is slow; gastroesophageal reflux; 50% fed by mouth; G-tube; vomiting once a month or more; acute neutropenia; acute anemia; immune deficiency; acute low platelets; asthma; broken bones: nondisplaced proximal right fibula and distal right radius; short stature; first walked at 18 months of age; language is slightly below age level; talked at 2 years of age; age appropriate cognitive ability; episodes of ketoacidosis once a month or more; on metabolic formula and levocarnitine; hypothyroid; esophagitis; fibroblast carboxylases results: propionyl-CoA carboxylase (PCC) 21 pmol/min/mg protein (normal range is 91-500), 3-methylcrotonyl-CoA carboxylase (MCC) 136 pmol/min/mg protein (normal range is 31-220), and pyruvate carboxylase (PC) 305 pmol/min/mg protein (normal range is 71-370); donor subject is homozygous for a 2 bp deletion at nucleotide 1172 in exon 11 of the PCCB gene (c.1172_1173delTT) |