Osteoarthropathy, Primary Hypertrophic [primární hypertrofická osteoartropatie]

topical
127
Terms

akropachie dědičná
kranioosteoartropatie
osteoartropatie primární hypertrofická
osteoartropatie primární hypertrofická autozomálně dominantní
pachydermoperiostosis
pachydermoperiostosis autozomálně dominantní
pachydermoperiostóza
paličkovité prsty kongenitální

 

Acropachy, Hereditary
Clubbing of Digits
Cranioosteoarthropathy
Currarino Idiopathic Osteoarthropathy
Digital Clubbing, Isolated Congenital
Familial Idiopathic Osteoarthropathy Of Childhood
Hypertrophic Osteoarthropathy, Primary, Autosomal Dominant
Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive
Idiopathic Hypertrophic Osteoarthropathy
Pachydermoperiostosis
Pachydermoperiostosis, Autosomal Dominant
Pachydermoperiostosis, Autosomal Recessive
Primary Hypertrophic Osteoarthropathy, Autosomal Dominant
Touraine-Solente-Gole Syndrome

Persistent link   https://www.medvik.cz/link/D010004
Definition

A condition chiefly characterized by thickening of the skin of the head and distal extremities, deep folds and furrows of the skin of the forehead, cheeks, and scalp, SEBORRHEA; HYPERHIDROSIS; periostosis of the long bones, digital clubbing, and spadelike enlargement of the hands and feet. It is more prevalent in the male, and is usually first evident during adolescence. Inheritance is primarily autosomal recessive, but an autosomal dominant form exists.

Annotation
OSTEOARTHROPATHY, SECONDARY HYPERTROPHIC is also available
DUI
D010004 MeSH Browser
CUI
M0015511
History note
2014(1964)
Public note
2012; see OSTEOARTHROPATHY, PRIMARY HYPERTROPHIC 1964-2013; CRANIOOSTEOARTHROPATHY was indexed under OSTEOARTHROPATHY, PRIMARY HYPERTROPHIC 2012-2013; DIGITAL CLUBBING, ISOLATED CONGENITAL was indexed under NAILS, MALFORMED 2012-2013; HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL DOMINANT was indexed under OSTEOARTHROPATHY, PRIMARY HYPERTROPHIC 2012-2013

C Diseases
C05.116 Bone Diseases 796
C05.116.070 Bone Cysts 78
C05.116.214 Bone Malalignment 16
C05.116.231 Bone Neoplasms 1 353
C05.116.264 Bone Resorption 344
C05.116.296 Coxa Magna
C05.116.327 Coxa Valga 1
C05.116.425 Epiphyses, Slipped 57
C05.116.482 Genu Valgum 12
C05.116.511 Genu Varum 2
C05.116.540 Hyperostosis 22
C05.116.680 Osteitis 43
C05.116.692 Osteitis Deformans 99
C05.116.791 Osteochondritis 122
C05.116.821 Osteochondrosis 12
C05.116.852 Osteonecrosis 190
C05.116.900 Spinal Diseases 1 240
C05.550 Joint Diseases 1 254
C05.550.069 Ankylosis 65
C05.550.091 Arthralgia 277
C05.550.114 Arthritis 827
C05.550.150 Arthrogryposis 31
C05.550.251 Bursitis 57
C05.550.323 Contracture 154
C05.550.445 Hallux Limitus 2
C05.550.450 Hallux Rigidus 26
C05.550.459 Hemarthrosis 63
C05.550.509 Hydrarthrosis 2
C05.550.518 Joint Dislocations 377
C05.550.521 Joint Instability 252
C05.550.535 Joint Loose Bodies 4
C05.550.610 Metatarsalgia 12
C05.550.870 Synovitis 172
C16.320.051 Alagille Syndrome 19
C16.320.100 Brugada Syndrome 40
C16.320.129 CADASIL 8
C16.320.165 CHARGE Syndrome 1
C16.320.170 Cherubism 1
C16.320.180 Chromosome Disorders 260
C16.320.184 Ciliopathies 9
C16.320.188 Costello Syndrome 3
C16.320.190 Cystic Fibrosis 1 330
C16.320.215 Donohue Syndrome 1
C16.320.240 Dwarfism 99
C16.320.306 Frasier Syndrome
C16.320.314 GATA2 Deficiency 2
C16.320.365 Hemoglobinopathies 68
C16.320.467 Kallmann Syndrome 10
C16.320.480 Kartagener Syndrome 46
C16.320.488 Laminopathies 2
C16.320.540 Marfan Syndrome 105
C16.320.577 Muscular Dystrophies 141
C16.320.728 Osteochondrodysplasias 125
C16.320.784 Pelger-Huet Anomaly 7
C16.320.812 Pycnodysostosis 2
C16.320.925 Werner Syndrome 14

Reginato Schiapachasse syndrome Disease MeSH Browser