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Descriptor English: Keratoderma, Palmoplantar, Diffuse
Descriptor Spanish: Queratodermia Palmar y Plantar Difusa
Descriptor queratodermia palmoplantar difusa
Entry term(s) queratodermia palmar y plantar difusa
síndrome de Thost-Unna
síndrome de Unna-Thost
tilosis
Scope note: Trastorno autosómico dominante que se caracteriza por presentar una hiperqueratosis ampliamente distribuida y bien delimitada en las palmas de las manos y plantas de los pies. Hay más de una forma genotípicamente diferente, cada una de las cuales es clinicamente similar pero distinguible histológicamente. La queratodermia palmoplantar difusa es diferente de la queratodermis palmoplantar (QUERATODERMIA PALMOPLANTAR), ya que la primera muestra frecuentemente una herencia autosómica dominante e hiperhidrosis.
Descriptor Portuguese: Ceratodermia Palmar e Plantar Difusa
Descriptor French: Kératodermie palmoplantaire diffuse
Entry term(s): Keratosis Palmaris et Plantaris Familiaris
Syndrome, Thost-Unna
Syndrome, Unna-Thost
Thost Unna Syndrome
Thost-Unna Syndrome
Tylosis
Unna Thost Syndrome
Unna-Thost Syndrome
Tree number(s): C16.320.850.475.440
C17.800.428.435.440
C17.800.827.475.440
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D015776
Scope note: An autosomal dominant disorder characterized by a widely distributed, well-demarcated hyperkeratosis of the palms and soles. There is more than one genotypically distinct form, each of which is clinically similar but histologically distinguishable. Diffuse palmoplantar keratoderma is distinct from palmoplantar keratoderma (KERATODERMA, PALMOPLANTAR), as the former exhibits autosomal dominant inheritance and hyperhidrosis is frequently present.
Annotation: do not confuse with KERATODERMA, PALMOPLANTAR
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Previous Indexing: Keratoderma, Palmoplantar (1974-1989)
Keratosis (1966-1973)
Public MeSH Note: 90
History Note: 90
DeCS ID: 24759
Unique ID: D015776
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1990/01/01
Date of Entry: 1989/10/19
Revision Date: 2015/06/18
Keratoderma, Palmoplantar, Diffuse - Preferred
Concept UI M0024171
Scope note An autosomal dominant disorder characterized by a widely distributed, well-demarcated hyperkeratosis of the palms and soles. There is more than one genotypically distinct form, each of which is clinically similar but histologically distinguishable. Diffuse palmoplantar keratoderma is distinct from palmoplantar keratoderma (KERATODERMA, PALMOPLANTAR), as the former exhibits autosomal dominant inheritance and hyperhidrosis is frequently present.
Preferred term Keratoderma, Palmoplantar, Diffuse
Entry term(s) Syndrome, Thost-Unna
Syndrome, Unna-Thost
Thost Unna Syndrome
Thost-Unna Syndrome
Tylosis
Unna Thost Syndrome
Unna-Thost Syndrome
Keratosis Palmaris et Plantaris Familiaris - Related but not broader or narrower
Concept UI M0574445
Preferred term Keratosis Palmaris et Plantaris Familiaris



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