Literature DB >> 23853024

Neurological improvement following reinstitution of a low phenylalanine diet after 20 years in established phenylketonuria.

M S Anwar1, B Waddell, J O'Riordan.   

Abstract

A 41-year-old woman had meaningful functional improvement following reinstitution of a low phenylalanine diet. She was diagnosed at birth with phenylketonuria and followed strict dietary adherence till the age of 16. Thereafter the diet was discontinued. She subsequently presented with subacute profound visual loss, cognitive dysfunction and paraparesis such that she was bed bound requiring full nursing care. Following dietary intervention there was meaningful improvement such that she was no longer demented and while her vision remains poor she is now independent for activities of daily living. This case report suggests that consideration of reimplementation of dietary intervention is warranted even after a prolonged period of time.

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Year:  2013        PMID: 23853024      PMCID: PMC3736477          DOI: 10.1136/bcr-2013-010509

Source DB:  PubMed          Journal:  BMJ Case Rep        ISSN: 1757-790X


  7 in total

Review 1.  Phenylketonuria.

Authors:  Nenad Blau; Francjan J van Spronsen; Harvey L Levy
Journal:  Lancet       Date:  2010-10-23       Impact factor: 79.321

2.  Musty odour, mental retardation, and spastic paraplegia revealing phenylketonuria in adulthood.

Authors:  Guillemette Jousserand; Jean-Christophe Antoine; Jean-Philippe Camdessanché
Journal:  J Neurol       Date:  2009-10-28       Impact factor: 4.849

3.  Effects of dietary management of phenylketonuria on long-term cognitive outcome.

Authors:  Shelley Channon; Galya Goodman; Sally Zlotowitz; Caroline Mockler; Philip J Lee
Journal:  Arch Dis Child       Date:  2006-10-26       Impact factor: 3.791

4.  The rehabilitation programme of an adult phenylketonuria with upper motor neuron involvement.

Authors:  Feray Soyupek; Hasan Koyuncuoglu; Abdullah Cindas; Erdem Ilgun; Rukiye Tak
Journal:  J Back Musculoskelet Rehabil       Date:  2009       Impact factor: 1.398

5.  Neurological complications and behavioral problems in patients with phenylketonuria in a follow-up unit.

Authors:  María J González; Alfonso P Gutiérrez; Rosa Gassió; María E Fusté; María A Vilaseca; Jaume Campistol
Journal:  Mol Genet Metab       Date:  2011-07-23       Impact factor: 4.797

6.  Do adult patients with phenylketonuria improve their quality of life after introduction/resumption of a phenylalanine-restricted diet?

Authors:  R Gassió; J Campistol; M A Vilaseca; N Lambruschini; F J Cambra; E Fusté
Journal:  Acta Paediatr       Date:  2003-12       Impact factor: 2.299

7.  Neurological deterioration in young adults with phenylketonuria.

Authors:  A J Thompson; I Smith; D Brenton; B D Youl; G Rylance; D C Davidson; B Kendall; A J Lees
Journal:  Lancet       Date:  1990-09-08       Impact factor: 79.321

  7 in total
  3 in total

1.  Altered visual functions, macular ganglion cell and papillary retinal nerve fiber layer thickness in early-treated adult PKU patients.

Authors:  Csilla Serfozo; Andras Gellert Barta; Endre Horvath; Csaba Sumanszki; Bela Csakany; Miklos Resch; Zoltan Zsolt Nagy; Peter Reismann
Journal:  Mol Genet Metab Rep       Date:  2020-09-22

Review 2.  The complete European guidelines on phenylketonuria: diagnosis and treatment.

Authors:  A M J van Wegberg; A MacDonald; K Ahring; A Bélanger-Quintana; N Blau; A M Bosch; A Burlina; J Campistol; F Feillet; M Giżewska; S C Huijbregts; S Kearney; V Leuzzi; F Maillot; A C Muntau; M van Rijn; F Trefz; J H Walter; F J van Spronsen
Journal:  Orphanet J Rare Dis       Date:  2017-10-12       Impact factor: 4.123

3.  Saccadic reaction time and ocular findings in phenylketonuria.

Authors:  Susanne Hopf; Caroline Nowak; Julia B Hennermann; Irene Schmidtmann; Norbert Pfeiffer; Susanne Pitz
Journal:  Orphanet J Rare Dis       Date:  2020-05-25       Impact factor: 4.123

  3 in total

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