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Items: 3

1.

Azorean disease

Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is characterized by progressive cerebellar ataxia and variable findings including pyramidal signs, a dystonic-rigid extrapyramidal syndrome, significant peripheral amyotrophy and generalized areflexia, progressive external ophthalmoplegia, action-induced facial and lingual fasciculations, and bulging eyes. Neurologic findings tend to evolve as the disorder progresses. [from GeneReviews]

MedGen UID:
9841
Concept ID:
C0024408
Disease or Syndrome
2.

Developmental and epileptic encephalopathy, 49

Developmental and epileptic encephalopathy-49 (DEE49) is a severe autosomal recessive neurologic disorder characterized by onset of seizures in the neonatal period, global developmental delay with intellectual disability and lack of speech, hypotonia, spasticity, and coarse facial features. Some patients may have brain calcifications on imaging (summary by Han et al., 2016). For a general phenotypic description and a discussion of genetic heterogeneity of DEE, see 308350. [from OMIM]

MedGen UID:
934602
Concept ID:
C4310635
Disease or Syndrome
3.

Facial-lingual fasciculations

Fasciculations affecting the tongue muscle and the musculature of the face. [from HPO]

MedGen UID:
354727
Concept ID:
C1862359
Finding
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