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Dive into the research topics where Ana Fortuna is active.

Publication


Featured researches published by Ana Fortuna.


Journal of inherited metabolic disorders reports | 2015

Infantile Refsum Disease: Influence of Dietary Treatment on Plasma Phytanic Acid Levels

Maria João Nabais Sá; J.C. Rocha; Manuela Almeida; Carla Carmona; E. Martins; Vasco Miranda; Miguel Coutinho; Rita Ferreira; Sara Pacheco; Francisco Laranjeira; Isaura Ribeiro; Ana Fortuna; Lúcia Lacerda

Infantile Refsum disease (IRD) is one of the less severe of Zellweger spectrum disorders (ZSDs), a group of peroxisomal biogenesis disorders resulting from a generalized peroxisomal function impairment. Increased plasma levels of very long chain fatty acids (VLCFA) and phytanic acid are biomarkers used in IRD diagnosis. Furthermore, an increased plasma level of phytanic acid is known to be associated with neurologic damage. Treatment of IRD is symptomatic and multidisciplinary.The authors report a 3-year-old child, born from consanguineous parents, who presented with developmental delay, retinitis pigmentosa, sensorineural deafness and craniofacial dysmorphisms. While the relative level of plasma C26:0 was slightly increased, other VLCFA were normal. Thus, a detailed characterization of the phenotype was essential to point to a ZSD. Repeatedly increased levels of plasma VLCFA, along with phytanic acid and pristanic acid, deficient dihydroxyacetone phosphate acyltransferase activity in fibroblasts and identification of the homozygous pathogenic mutation c.2528G>A (p.Gly843Asp) in the PEX1 gene, confirmed this diagnosis. Nutritional advice and follow-up was proposed aiming phytanic acid dietary intake reduction. During dietary treatment, plasma levels of phytanic acid decreased to normal, and the patients development evaluation showed slow progressive acquisition of new competences.This case report highlights the relevance of considering a ZSD in any child with developmental delay who manifests hearing and visual impairment and of performing a systematic biochemical investigation, when plasma VLCFA are mildly increased. During dietary intervention, a biochemical improvement was observed, and the long-term clinical effect of this approach needs to be evaluated.


Blood Cells Molecules and Diseases | 1999

T cell numbers relate to bone involvement in Gaucher disease.

Lúcia Lacerda; Fernando A. Arosa; Rosa Lacerda; José Manuel Cabeda; Graça Porto; Olga Amaral; Ana Fortuna; Rui Pinto; Pedro Oliveira; Christine E. McLaren; Clara Sá Miranda; Maria de Sousa


Revista Portuguesa De Pneumologia | 2003

Cervical aortic arch and 22q11 deletion--the role of MRI in diagnosis.

Rui Almeida; Sílvia Álvares; Ana Fortuna; Jorge Moreira; Vieira A


NASCER E CRESCER - BIRTH AND GROWTH MEDICAL JOURNAL | 2016

A NOVEL MISSENSE MUTATION IN THE ALPHATROPOMYOSIN (TPM1) GENE IN A FAMILY AFFECTED WITH HYPERTROPHIC CARDIOMYOPATHY

Emília Vieira; Márcia E. Oliveira; Nataliya Tkachenko; Sílvia Álvares; José Carlos Machado; Ana Fortuna; Rosário Santos


NASCER E CRESCER - BIRTH AND GROWTH MEDICAL JOURNAL | 2016

THE CLINICAL AND NEUROCOGNITIVE FEATURES OF DIGEORGE SYNDROME PATIENTS OF CENTRO DE GENÉTICA MÉDICA DOUTOR JACINTO MAGALHÃES

Carla Carmona; Mariana R. Pereira; Gabriela Soares; Maria João Nabais; Natalyia Tkachenko; Ana Fortuna


NASCER E CRESCER - BIRTH AND GROWTH MEDICAL JOURNAL | 2016

FABRY DISEASE IN PORTUGAL – INSIGHTS FROM THE MALE PATIENTS

Ana Rita Soares; Francisco Laranjeira; Carla Caseiro; Isaura Ribeiro; Elisabete Silva; Eugénia Pinto; Célia Ferreira; Sónia Rocha; Ana Fortuna; Dulce Quelhas; Lúcia Lacerda


European Journal Human Genetics Conference, 21-24 May 2016 | 2016

Early results of next-gen cytogenetics implementation in Portugal

Dezső David; João Freixo; Bárbara Marques; Inês Carvalho; Natália Tkachenko; Natália Oliva-Teles; Mariana Marques; Manuela Pinto Cardoso; Joana Fino; Cristina Alves; Ana Fortuna; Dória Sófia; Carla Pinto de Moura; Hildeberto Correia; Isabel M. Carreira; Joaquim de Sá; Rui Gonçalves; João Lavinha; Teresa Kay; Michael E. Talkowski; Cynthia C. Morton


Nascer e Crescer | 2015

High phenotypic variability in two siblings with spinal muscular atrophy

Teresa Saraiva; Jorge Oliveira; Márcia E. Oliveira; Ana Sofia Soares; Rosário Santos; Ana Fortuna


19ª Reunião da Sociedade Portuguesa de Genética Humana, 5-7 novembro 2015 | 2015

Next-Gen Cytogenetics and the Hidden Complexity of Genomic or Chromosomal Rearrangements

Dezső David; João Freixo; Inês Carvalho; Natália Tkachenko; Natália Oliva Teles; Bárbara Marques; Ana Cristina Alves; Ana Fortuna; Dória Sófia; Carla Pinto de Moura; Isabel Mendes Gaspar; Isabel M. Carreira; Joaquim de Sá; Rui Gonçalves; João Lavinha; Teresa Kay; Hildeberto Correia; Michael E. Talkowski; Cynthia C. Morton


Nascer e Crescer | 2014

Trisomy x syndrome (47,XXX) preventive management in pediatric age: case report

T Saraiva; Fernanda Paula Oliveira; N. Oliva Teles; M.L. Fonseca e Silva; Ana Fortuna

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Lúcia Lacerda

Instituto Nacional de Saúde Dr. Ricardo Jorge

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Bárbara Marques

Instituto Nacional de Saúde Dr. Ricardo Jorge

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Dezső David

Instituto Nacional de Saúde Dr. Ricardo Jorge

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Hildeberto Correia

Instituto Nacional de Saúde Dr. Ricardo Jorge

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João Lavinha

Instituto Nacional de Saúde Dr. Ricardo Jorge

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Márcia E. Oliveira

Instituto de Biologia Molecular e Celular

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