New to this group with a couple of questions

[Guest guest]

Hi, I was referred to this group by metabolic disorders. I have 3

children ages 5, 9, and 12. My two oldest are boys. My oldest has LDs

in reading, math, writing, language/speech, hypotonia, under the 3%

for weight, 5% for height, anxiety disorder, and has connective

tissue disorder. He has long slender arms, long legs, long thin

fingers, and long toes along with long narrow feet. His urine amino

acids came back elevated twice for glycine.

MY nine yr old has autism, asthma, allergies, LDs, complex partial

seizures, sensory issues, hypotonia, speech/language delays, tics,

and ADD. My 5 yr old also has autism, LDs, sensory issues,

generalized seizures(tic-like & myoclonic), speech/language delays,

and pica.

I have seizures(multiple types), celiac disease, and sometime low

blood sugar. My mother had schzophrenia, as did her brother and

father. She also had diabetes, heart disease, and glacoma.

My husband has diabetes, CLL Leukemia, and family history of

diabetes, MS, Food allergies, asthma, heart attack and stroke.

Does anyone know the references for umol/L for amino acids random

urine screening. I have the labs back but not the references.