Diagnosis and Management of Classical Homocystinuria in Brazil: A Summary of 72 Late-Diagnosed Patients. (7th August 2018)
- Record Type:
- Journal Article
- Title:
- Diagnosis and Management of Classical Homocystinuria in Brazil: A Summary of 72 Late-Diagnosed Patients. (7th August 2018)
- Main Title:
- Diagnosis and Management of Classical Homocystinuria in Brazil
- Authors:
- Poloni, Soraia
Hoss, Giovana W.
Sperb-Ludwig, Fernanda
Borsatto, Taciane
Doriqui, Maria Juliana R.
Leão, Emília K.E.A
Boa-Sorte, Ney
Lourenço, Charles M.
Kim, Chong A.
de Souza, Carolina F. M.
Rocha, Helio
Ribeiro, Marcia
Steiner, Carlos E.
Moreno, Carolina A.
Bernardi, Pricila
Valadares, Eugenia
Artigalas, Osvaldo
Carvalho, Gerson
Wanderley, Hector Y. C.
D'Almeida, Vânia
Santana-da-Silva, Luiz C.
Blom, Henk J.
Schwartz, Ida V. D. - Abstract:
- This study described a broad clinical characterization of classical homocystinuria (HCU) in Brazil. This was a cross-sectional, observational study including clinical and biochemical data from 72 patients (60 families) from Brazil (South, n = 13; Southeast, n = 37; Northeast, n = 8; North, n = 1; and Midwest, n = 1). Parental consanguinity was reported in 42% of families. Ocular manifestations were the earliest detected symptom (53% of cases), the main reason for diagnostic suspicion (63% of cases), and the most prevalent manifestation at diagnosis (67% of cases). Pyridoxine responsiveness was observed in 14% of patients. Only 22% of nonresponsive patients on treatment had total homocysteine levels <100 µmol/L. Most commonly used treatment strategies were pyridoxine (93% of patients), folic acid (90%), betaine (74%), vitamin B12 (27%), and low-methionine diet + metabolic formula (17%). Most patients diagnosed with HCU in Brazil are late diagnosed, express a severe phenotype, and poor metabolic control. Milder forms of HCU are likely underrepresented due to underdiagnosis.
- Is Part Of:
- Journal of inborn errors of metabolism and screening. Volume 6(2018)
- Journal:
- Journal of inborn errors of metabolism and screening
- Issue:
- Volume 6(2018)
- Issue Display:
- Volume 6, Issue 2018 (2018)
- Year:
- 2018
- Volume:
- 6
- Issue:
- 2018
- Issue Sort Value:
- 2018-0006-2018-0000
- Page Start:
- Page End:
- Publication Date:
- 2018-08-07
- Subjects:
- classical homocystinuria -- CBS deficiency -- homocysteine -- pyridoxine responsiveness -- diagnosis
Metabolism, Inborn errors of -- Periodicals
Metabolism, Inborn errors of -- Diagnosis -- Periodicals
616.3904205 - Journal URLs:
- http://www.jiems-journal.org/ ↗
http://www.uk.sagepub.com ↗ - DOI:
- 10.1177/2326409818788900 ↗
- Languages:
- English
- ISSNs:
- 2326-4594
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 9608.xml