Oculocerebrorenal syndrome

Lowe Oculocerebrorenal Syndrome
Charles Upton Lowe, an American pediatrician, reported three boys with the characteristics of this syndrome in 1952. It is sometimes called Lowe syndrome, or oculo-cerebro-renal syndrome.
Clinical Correlations ...

acidemia, 3-Methylcrotonyl-CoA carboxylase deficiency), IBD deficiency - Straight-chain (Hyperlysinemia, Pipecolic acidemia, Saccharopinuria) - Transport (Cystinuria, Cystinosis, Hartnup disease, Fanconi syndrome, Oculocerebrorenal syndrome, ...

oculocerebrorenal syndrome
oculocutaneous syndrome
oculomandibulofacial syndrome
oculopharyngeal syndrome
oculovertebral syndrome
oculovestibulo-auditory syndrome
OFD syndrome
Ogilvie's syndrome
Omenn's syndrome
onychoosteodysplasia ...

oculocerebrorenal syndrome
oculocerebrorenal syndrome of Lowe
oculocutaneous albinism type 1B
Oculocutaneous Albinism, Chediak-Higashi Type
Oculodentodigital Dysplasia
Oculomandibulodyscephaly with hypotrichosis
Oculomandibulofacial syndrome ...

gamma-Linolenic Acid, Ammonium Salt, Glycoside Antibiotics, IGF II Receptor, Infarctions, Injection, Epidural, Interleukin 6, Inwardly Rectifying Potassium Channel, Joint, Intermetatarsal, K Cell, Kangaroo, Rat, LATS, Lowe Oculocerebrorenal Syndrome, ...

Scriver's Online Metabolic and Molecular Bases of Inherited Disease (OMMBID): The Oculocerebrorenal Syndrome of Lowe (Lowe Syndrome)
OMIM - Genetic disorder catalog
What other names do people use for Lowe syndrome?

Lowe oculocerebrorenal syndrome ... excess protein in urine, excess amino acids in urine, excess amino acids in urine
Lowe Syndrome ... Excess protein in urine, Excess amino acids in urine, Excess amino acids in urine
Lubinsky syndrome ...

See also: Deficiency, Albinism, Fanconi syndrome, Malabsorption, Lesch-Nyhan syndrome