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Fazio–Londe disease

Fazio–Londe disease
Classification and external resources
ICD-10 G12.1
ICD-9-CM 335.2
OMIM 211500
DiseasesDB 29491
MeSH D010244

Fazio–Londe disease (FLD), also called progressive bulbar palsy of childhood,[1][2] is an very rare inherited motor neuron disease of children and young adults and is characterized by progressive paralysis of muscles innervated by cranial nerves.


  • Signs and symptoms 1
  • Genetics 2
  • Prognosis 3
  • History 4
  • Eponym 5
  • References 6
  • External links 7

Signs and symptoms

FLD produces rapidly progressive weakness of tongue, face and pharyngeal muscles in a clinical pattern similar to myasthenia. Neuromuscular transmission may be abnormal in these muscles because of rapid denervation and immature reinnervation. Paralysis occurs secondary to degeneration of the motor neurons of the brain stem. It causes progressive bulbar paralysis due to involvement of motor neurons of the cranial nerve nuclei. The most frequent symptoms at onset of progressive bulbar paralysis of childhood has been a unilateral facial paralysis. It is followed in frequency by dysarthria due to facial weakness or by dysphagia. Palatal weakness and palpebral ptosis also have been reported in few patients. Both sexes can be affected.


Autosomal recessive mode of inheritance

Fazio–Londe disease is linked to a genetic mutation in the SLC52A3 gene on chromosome 20 (locus: 20p13).[1] It is allelic and phenotypically similar to Brown–Vialetto–Van Laere syndrome.[3][1]

The condition is inherited in an autosomal recessive manner.[1]


Onset of first symptom has been reported between 1–12 years, with a mean age of onset at 8 years. Clinical course can be divided into early (< 6 yrs age, predominance of respiratory symptoms) and late course (6–20 years of age, predominance of motor symptoms on superior limbs). Progression to involve other cranial nerve muscles occurs over a period of months or years. In the Gomez review facial nerve was affected in all cases while hypoglossal nerve was involved in all except one case. Other cranial nerves involved were vagus, trigeminal, spinal accessory nerve, abducent, occulomotor and glossopharyngeal in this order. Corticospinal tract signs were found in 2 of the 14 patients.

The disease may progress to patient's death in a period as short as 9 months or may have a slow evolution or may show plateaus. Post mortem examination of cases have found depletion of nerve cells in the nuclei of cranial nerves. The histologic alterations found in patient with Fazio–Londe disease were identical to those seen in infantile-onset spinal muscular atrophy.

Strength may improve with administration of cholinesterase inhibitors.


Berger, in 1876, first reported a case of 12-year-old child with progressive bulbar paralysis


It is named for E. Fazio and Paul Londe.[4][5]


  1. ^ a b c d Online 'Mendelian Inheritance in Man' (OMIM) 211500
  2. ^ "progressive bulbar palsy of childhood" at Dorland's Medical Dictionary
  3. ^ Dipti S, Childs AM, Livingston JH; et al. (September 2005). "Brown–Vialetto–Van Laere syndrome; variability in age at onset and disease progression highlighting the phenotypic overlap with Fazio–Londe disease". Brain Dev. 27 (6): 443–446.  
  4. ^ synd/1909 at Who Named It?
  5. ^ Londe, P. Paralysie bulbaire progressive, infantile et familiale. Rev. Med. 14: 212–254, 1894.

External links

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