Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome

Eugenio Maria Mercuri, Serenella Servidei, Tommaso Verdolotti, Guido Alessandro Primiano, Orazio Genovese, Roberta Battini, Giorgia Olivieri, Roberta Milone, Federica Mazio, Roberta Scalise

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

Background: Biotinidase deficiency (BTD) is an autosomal recessive inborn error of metabolism provoking progressive biotin depletion, which causes, in turn, multiple carboxylase deficiency. Its infantile onset is characterized by intractable seizures associated with lethargy, psychomotor regression, hypotonia, feeding and respiratory problems, and cutaneous abnormalities. Case description: We describe a 52-month-old female whose clinical and neuroradiological pictures were consistent with myelopathy, which is generally more frequent in older patients, as well as with symptoms of an infantile onset of biotinidase deficiency, revealed at 17 months. Results: A biochemical biotinidase test revealed a profound deficiency of biotinidase detecting a 10% residual enzymatic activity, which led to the diagnosis of BTD. Gene sequencing revealed a compound heterozigous mutation (c.454A > C/c.1612C > T). Conclusion: Our findings suggest that even if myelopathy is uncommonly reported in BTD, and generally occurs in older children, its presence in childhood-onset floppiness should always be considered as a possible marker for an atypical presentation of BTD. Although, until recently, BTD myelopathy was believed to be prevalent in older children, a spinal cord involvement has also been described in at least nine cases in early infancy. Thus, another early diagnosis suggests that myelopathy may be more frequent than previously thought, and it is probably underdiagnosed because spinal MRI is not always routinely performed on these children. Early recognition of BTD disease is important as it would lead to prompt treatment, preventing irreversible brain damage and increasing the chances of complete recovery.
Lingua originaleEnglish
pagine (da-a)N/A-N/A
Numero di pagine5
RivistaBRAIN & DEVELOPMENT
Volume2020
DOI
Stato di pubblicazionePubblicato - 2020

Keywords

  • Biotinidase defect
  • Childhood-onset
  • Demyelinating spinal cord
  • Multiple sclerosis
  • Treatable epilepsy

Fingerprint Entra nei temi di ricerca di 'Spinal cord demyelination in children: A diagnostic challenge in neuropaediatrics for a good outcome'. Insieme formano una fingerprint unica.

Cita questo