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Keratosis Follicularis

Known as: DD, WHITE-DARIER DISEASE, Follicular keratosis 
An autosomal dominantly inherited skin disorder characterized by warty malodorous papules that coalesce into plaques. It is caused by mutations in… 
National Institutes of Health

Related topics

Related topics

29 relations
ATP2A2 geneAcantholytic Dyskeratotic Epidermal NevusAcrokeratosis Verruciformis of HopfAutosomal dominant inheritance

Narrower (5)

Burnett Schwartz Berberian syndromeKERATOSIS FOLLICULARIS SPINULOSA DECALVANS, AUTOSOMAL DOMINANT (disorder)Keratosis follicularis dwarfism cerebral atrophyKyrle disease

Broader (4)

Hereditary DiseasesKeratinization, functionKeratosisTyloma

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Estimated Prevalence of Autism and Other Developmental Disabilities Following Questionnaire Changes in the 2014 National Health Interview Survey.
OBJECTIVES The developmental disabilities questions in the 2014 National Health Interview Survey (NHIS) were changed from… 
Highly Cited
2011
Highly Cited
2011
Elevated plasma cytokines in autism spectrum disorders provide evidence of immune dysfunction and are associated with impaired behavioral outcome
Highly Cited
2006
Highly Cited
2006
Sensory Experiences Questionnaire: discriminating sensory features in young children with autism, developmental delays, and typical development.
BACKGROUND This study describes a new caregiver-report assessment, the Sensory Experiences Questionnaire (SEQ), and explicates… 
Highly Cited
2004
Highly Cited
2004
Early Indicators of Autism Spectrum Disorders in the Second Year of Life
Three groups of 18 children were selected for this study, one group with autism spectrum disorders (ASD), one group with… 
Highly Cited
2004
Highly Cited
2004
Delay discounting and probability discounting as related to cigarette smoking status in adults
Review
2001
Review
2001
How Much Should We Trust Differences-in-Differences Estimates?
Most Difference-in-Difference (DD) papers rely on many years of data and focus on serially correlated outcomes. Yet almost all… 
Highly Cited
2000
Highly Cited
2000
Mutations in ATP2C1, encoding a calcium pump, cause Hailey-Hailey disease
Hailey-Hailey disease (HHD, MIM 16960) is inherited in an autosomal dominant manner and characterized by persistent blisters and… 
Highly Cited
1999
Highly Cited
1999
Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease
Darier disease (DD) is an autosomal-dominant skin disorder characterized by loss of adhesion between epidermal cells… 
Highly Cited
1996
Highly Cited
1996
A meta-analysis of the association of the deletion allele of the angiotensin-converting enzyme gene with myocardial infarction.
BACKGROUND The ACE gene is characterized by a polymorphism based on the presence (insertion [I]) or absence (deletion [D]) within… 
Highly Cited
1993
Highly Cited
1993
Mistyping ACE heterozygotes.
Depar tment of Pathology, Emory University School of Medicine, Atlanta, Georgia 30322 Human angiotensin I-converting enzyme (ACE… 
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