Pseudodominance in Friedreich Ataxia—Impact of High Prevalence of Carriers and Intrafamilial Clinical Variation

• Published in: Movement disorders clinical practice (Hoboken, N.J.) Vol. 10; no. 4; pp. 670 - 676
• Main Authors: Malaquias, Maria João, Oliveira, Jorge, Santos, Manuela, Brandão, Ana Filipa, Sardoeira, Ana, Sequeiros, Jorge, Barros, José, Damásio, Joana
• Format: Journal Article
• Language: English
• Published: Hoboken, USA John Wiley & Sons, Inc 01.04.2023; Wiley Subscription Services, Inc
• Subjects: Ataxia; Case Series with Literature Review; heterozygous carriers for recessive diseases; late‐onset Friedreich ataxia; pseudodominance; heterozygous carriers for recessive diseases; pseudodominance; late‐onset Friedreich ataxia
• ISSN: 2330-1619; 2330-1619
• DOI: 10.1002/mdc3.13694

ABSTRACT Background Friedreich ataxia (FA) is the most common form of autosomal recessive (AR) ataxia. It is a rare disease, but carriers are frequent (1/100). Pseudodominance in FA has seldomly been reported; it may pose additional challenges for diagnosis. Cases A family with two consecutive generations affected by FA is described. The proband and two younger siblings had typical FA, characterized by infantile‐onset ataxia, hyporeflexia, Babinski sign, cardiomyopathy, and loss of ambulation in the second decade of life. Another female sibling had delayed‐onset (>25 years old), with mild cerebellar and sensitive ataxia since her mid‐30s. Their father presented very late‐onset FA (>40 years old), with sensitive axonal neuropathy. All five patients had biallelic (GAA)n expansion in FXN. The first three had larger expansions (>800 repeats), while the latter two had one shorter expanded allele (~90 repeats). Literature Review Pseudodominant inheritance has been described in 13 neurological disorders. Seven are movement disorders, of which three were associated with high frequency of carriers (FA, Wilson's disease and PRKN‐related parkinsonism). Conclusions Clinicians should be aware of the possibility of pseudodominance when facing an apparent autosomal dominant pedigree, particularly in disorders with high frequency of carriers and variable expression. Otherwise, genetic diagnoses may be delayed.