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Dystrophia unguium

Known as: Dystrophic nails, dystrophic nail, NAIL DYSTROPHY 
Deformity or discoloration of a fingernail or toenail.(NICHD)
National Institutes of Health

Related topics

Related topics

40 relations
Anonychia-onychodystrophy with hypoplasia or absence of distal phalangesBloch Sulzberger syndromeCATARACT-ALOPECIA-SCLERODACTYLY SYNDROMECronkhite-Canada Syndrome

Broader (1)

Nail Diseases

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Advancing epilepsy genetics in the genomic era
Epilepsy is a group of disorders characterized by recurrent seizures, and is one of the most common neurological conditions. The… 
Review
2014
Review
2014
Managing Patients with Psoriatic Disease: The Diagnosis and Pharmacologic Treatment of Psoriatic Arthritis in Patients with Psoriasis
Psoriatic arthritis (PsA) is a chronic, systemic inflammatory disease. Up to 40 % of patients with psoriasis will go on to… 
Highly Cited
2013
Highly Cited
2013
Keratin 16 regulates innate immunity in response to epidermal barrier breach
Significance Here we report that keratin 16 (Krt16), a type I intermediate filament cytoskeletal protein, is an integral and… 
Highly Cited
2008
Highly Cited
2008
A hypomorphic mouse model of dystrophic epidermolysis bullosa reveals mechanisms of disease and response to fibroblast therapy.
Dystrophic epidermolysis bullosa (DEB) is a severe skin fragility disorder associated with trauma-induced blistering, progressive… 
Highly Cited
2003
Highly Cited
2003
Neuropathology with Clinical Correlations of Sporadic Amyotrophic Lateral Sclerosis: 102 Autopsy Cases Examined Between 1962 and 2000
Sporadic amyotrophic lateral sclerosis (ALS) is a fatal neurological disorder affecting adults. We studied the neuropathology and… 
Highly Cited
2001
Highly Cited
2001
Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.
Hay-Wells syndrome, also known as ankyloblepharon-ectodermal dysplasia-clefting (AEC) syndrome (OMIM 106260), is a rare autosomal… 
Highly Cited
1999
Highly Cited
1999
X-linked dyskeratosis congenita is predominantly caused by missense mutations in the DKC1 gene.
Dyskeratosis congenita is a rare inherited bone marrow-failure syndrome characterized by abnormal skin pigmentation, nail… 
Highly Cited
1999
Highly Cited
1999
Alopecia areata investigational assessment guidelines
Highly Cited
1998
Highly Cited
1998
A mutation in human keratin K6b produces a phenocopy of the K17 disorder pachyonychia congenita type 2.
Type I and type II keratins form the heteropolymeric intermediate filament cytoskeleton, which is the main stress-bearing… 
Review
1991
Review
1991
Bazex Syndrome (Acrokeratosis Paraneoplastica) An Analytic Review
Bazex syndrome (acrokeratosis paraneoplastica) is characterized by a psoriasiform eruption that favors acral sites and has been… 
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