aciduria

(redirected from Glutaric aciduria)
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Related to Glutaric aciduria: glutaric aciduria type 2

ac·i·du·ri·a

 (ăs′ĭ-do͝or′ē-ə, -dyo͝or′-)
n.
A condition marked by the presence of acid in the urine.

aciduria

(ˌæsɪdˈjʊərɪə)
n
the condition of having acid in the urine, particularly at abnormally high levels
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References in periodicals archive ?
Opercular abnormalities may be caused by genetic factors, as usually seen in Miller-Dieker syndrome,[sup][23] glutaric aciduria type 1,[sup][24],[25] methylmalonic acidaemia,[sup][26] and nonsyndromic microencephaly.
Food preparation) ga gel cpv 15880000-0 ga gel, Powdered lysine free and low tryptophan protein substitute, Containing essential and non essential amino acids, Carbohydrate, Vitamins, Minerals and trace elements, For the dietary management of glutaric aciduria type 1 (ga 1) from 1 to 10 years of age.
MADD was initially referred to as glutaric aciduria type II (GA II) to distinguish it from glutaric aciduria type I (GA I).
Other children included Matilda Hatton, from Walsall, who is one of an estimated 20 people to have Sensenbrenner Syndrome, siblings Noah and Ruby Harvey, from West Bromwich, who both have Glutaric Aciduria Type 1, and Skye Gardner, from Wednesbury who has Williams Syndrome.
Leigh's disease 13 MLD 4 Wilson's disease 2 Gangliosidosis 2 PKAN (NBIA Type 1) 2 Canavan's disease 1 Alexander's disease 1 Glutaric aciduria 1
Furthermore, from observations made on other inherited metabolic disorders, such as type 1 glutaric aciduria, galactosaemia and cystinosis, [16-18] it is becoming increasingly evident that the mutations commonly reported do not appear to reflect the disease-causing mutations among black African populations.
Two patients, one with glutaric aciduria type 1 and one with chronic liver disease died of ARDS.
The Newborn Blood Spot Screening Programme has been extended from January 5, to screen for an additional four rare, but potentially disabling, conditions which are homocystinuria (HCU), maple syrup urine disease (MSUD), glutaric aciduria type 1 (GA1) and isovaleric acidaemia (IVA).
From early next year, 'heel prick' blood samples taken from newborn babies will be tested for four additional metabolic disorders - glutaric aciduria type 1, homocystinuria, isovaleric acidaemia and maple syrup urine disease.
The NHS Newborn Blood Spot Screening programme will be expanded to screen for homocystinuria (HCU), maple syrup urine disease (MSUD), glutaric aciduria type 1 (GA1) and isovaleric acidaemia (IVA).
Glutaric aciduria type 1 is a rare inherited organic academia.