Abstract:
:A forme fruste Rett variant female with partially preserved speech remnants is described. She was first seen by the author at an age of 4 years. She then presented with an unspecific syndrome of moderate mental retardation. At follow-up when aged 32 she had successively through the years developed a number of Rett characteristic abnormal behavioural patterns and neurologic deviations, together convincingly indicating a Rett syndrome. However, this has been discrete and atypical in original presentation and first apparent in the long term clinical profile. It is underlined that a whole battery of Rett peculiarities appearing with age should be present to allow diagnostic accuracy.
journal_name
Neuropediatricsjournal_title
Neuropediatricsauthors
Hagberg Bdoi
10.1055/s-2007-979730subject
Has Abstractpub_date
1995-04-01 00:00:00pages
83-4issue
2eissn
0174-304Xissn
1439-1899journal_volume
26pub_type
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