Journal Article

New insights into the clinical and molecular spectrum of the MADD-related neurodevelopmental disorder

Abdel-Salam, Ghada M. H., Abdel-Hamid, Mohamed S.

2024

Overview

Biallelic pathogenic variants in MADD lead to a very rare neurodevelopmental disorder which is phenotypically pleiotropic grossly ranging from severe neonatal hypotonia, failure to thrive, multiple organ dysfunction, and early lethality to a similar but milder phenotype with better survival. Here, we report 5 patients from 3 unrelated Egyptian families in whom 4 patients showed the severe end of the spectrum displaying neonatal respiratory distress, hypotonia and chronic diarrhea while one patient presented with the mild form displaying moderate intellectual disability and myopathy. In addition, we observed distal arthrogryposis and nonspecific structural brain anomalies in all our patients. Interestingly, cerebellar and brainstem hypoplasia were noted in one patient. Whole exome sequencing identified three novel homozygous variants in the MADD gene: two likely pathogenic [c.4321delC p.(Gln1441ArgfsTer46) and c.2620 C > T p.(Arg874Ter)] and one variant of uncertain significance (c.4307 G > A, p.Arg1436Gln). The variants segregated with the disease in all available family members. Our findings confirm that arthrogryposis, genital, cardiac and structural brain anomalies are manifestations of MADD which expand the spectrum of MADD -related neurodevelopmental disorder. Moreover, they further highlight the convergence of MADD variants on different organ systems leading to complex phenotypes.

• Publisher: Nature Publishing Group,Springer Nature Singapore
• Subject: Arthrogryposis / Arthrogryposis - genetics / Arthrogryposis - pathology / Brain - abnormalities / Brain - pathology / Brain stem / Cerebellum / Child / Child, Preschool / Diarrhea / Egypt / Exome Sequencing / Female / Homozygote / Humans / Hypoplasia / Infant / Infant, Newborn / Intellectual disabilities / Intellectual Disability - genetics / Intellectual Disability - pathology / Lethality / Male / Muscle Hypotonia - genetics / Muscle Hypotonia - pathology / Mutation / Myopathy / Neonates / Neurodevelopmental disorders / Neurodevelopmental Disorders - genetics / Neurodevelopmental Disorders - pathology / Patients / Pedigree / Phenotype / Phenotypes