Pachyonychia congenita type I is an autosomal dominant disorder where nail abnormalities are a constant feature and develop during childhood. We report here a family with pachyonychia congenita type I and very mild nail changes to underline that this diagnosis should be considered even in the absence of severe nail thickening.

The nature of forgetting in short-term memory remains a disputed topic, with much debate focussed upon whether decay plays a fundamental role (Berman et al., 2009; Altmann and Schunn, 2012; Barrouillet et al., 2012; Neath and Brown, 2012; Oberauer and Lewandowsky, 2013; Ricker et al., 2014) but much less focus on other plausible mechanisms. One such mechanism of long-standing in auditory memory...

This introductory article to the Journal of Memory and Language special issue on memory models discusses the progress made in the field of memory modeling during the last few decades in terms of a number of previously suggested criteria, using the articles in this issue as examples. There has been considerable progress, both at a technical level (e.g., concerning model comparison and model anal...

Farrell and Lewandowsky (2008) argued that the temporal context model (TCM; Howard & Kahana, 2002) cannot explain nonmonotonicities in the contiguity effect seen at extreme lags. However, TCM actually predicts these nonmonotonicities to the extent that end-of-list context persists as a retrieval cue during recall and to the extent that end-of-list context generates a recency effect. We show tha...

Pachyonychia congenita (PC) is a group of hereditary syndromes which have in common a hypertrophic dystrophy of the distal nail, and are associated with a variety of additional features, notably various dyskeratoses of skin and mucous membranes. The pathology is unknown but the array of clinical features suggests the possibility of a keratin abnormality. In the present report we describe linkag...