Proteus Syndrome [Proteův syndrom]

topical
8
Terms

Proteus-like syndrom
syndrom hamartoneoplastický malformační
syndrom podobný Proteovu syndromu

 

Elephant Man Disease
Proteus-Like Syndrome

Persistent link   https://www.medvik.cz/link/D016715
Definition

Hamartoneoplastic malformation syndrome of uncertain etiology characterized by partial GIGANTISM of the hands and/or feet, asymmetry of the limbs, plantar hyperplasia, hemangiomas (HEMANGIOMA), lipomas (LIPOMA), lymphangiomas (LYMPHANGIOMA), epidermal NEVI; MACROCEPHALY; cranial HYPEROSTOSIS, and long-bone overgrowth. Joseph Merrick, the so-called elephant man, apparently suffered from Proteus syndrome and not NEUROFIBROMATOSIS, a disorder with similar characteristics.

Annotation
hamartomas & multiple abnorm; "Proteus" refers to the sea god in Greek mythol who could assume many forms; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D016715 MeSH Browser
CUI
M0025456
Previous indexing
Abnormalities, Multiple (1979-1991); Neoplasms, Multiple Primary (1986-1991); Neurofibromatosis 1 (1979-1990)
History note
92
Public note
92

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications
DI
diagnosis 3
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology 1
EP
epidemiology
EH
ethnology
ET
etiology 1
GE
genetics 2
HI
history
IM
immunology
ME
metabolism
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 2
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy
UR
urine
VE
veterinary
VI
virology

C Diseases
C04 Neoplasms 12 832
C04.445 Hamartoma 128
C04.445.435 Hamartoma Syndrome, Multiple 25
C04.445.435.500 Proteus Syndrome 8
C04.651 Neoplasms, Multiple Primary 159
C04.651.435 Hamartoma Syndrome, Multiple 25
C04.651.435.500 Proteus Syndrome 8
C05 Musculoskeletal Diseases 1 125
C05.116 Bone Diseases 796
C05.116.099 Bone Diseases, Developmental 293
C05.116.099.052 Acro-Osteolysis 3
C05.116.099.105 Basal Cell Nevus Syndrome 33
C05.116.099.343 Dwarfism 99
C05.116.099.370 Dysostoses 22
C05.116.099.386 Funnel Chest 38
C05.116.099.492 Gigantism 14
C05.116.099.655 Leg Length Inequality 118
C05.116.099.674 Marfan Syndrome 105
C05.116.099.708 Osteochondrodysplasias 125
C05.116.099.736 Osteolysis, Essential 8
C05.116.099.739 Pectus Carinatum 1
C05.116.099.742 Platybasia 12
C05.116.099.750 Proteus Syndrome 8
C05.660 Musculoskeletal Abnormalities 107
C05.660.585 Limb Deformities, Congenital 126
C05.660.585.174 Arachnodactyly 17
C05.660.585.262 Brachydactyly 4
C05.660.585.350 Ectromelia 23
C05.660.585.512 Lower Extremity Deformities, Congenital 56
C05.660.585.600 Polydactyly 31
C05.660.585.620 Proteus Syndrome 8
C05.660.585.800 Syndactyly 24
C05.660.585.984 Thanatophoric Dysplasia 7
C05.660.585.988 Upper Extremity Deformities, Congenital 14
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.077 Abnormalities, Multiple 330
C16.131.077.019 22q11 Deletion Syndrome 2
C16.131.077.065 Alagille Syndrome 19
C16.131.077.095 Angelman Syndrome 35
C16.131.077.121 Barth Syndrome 6
C16.131.077.130 Basal Cell Nevus Syndrome 33
C16.131.077.133 Beckwith-Wiedemann Syndrome 17
C16.131.077.137 Bloom Syndrome 11
C16.131.077.208 Branchio-Oto-Renal Syndrome 5
C16.131.077.229 Carney Complex 8
C16.131.077.245 Ciliopathies 9
C16.131.077.250 Cockayne Syndrome 4
C16.131.077.256 Costello Syndrome 3
C16.131.077.262 Cri-du-Chat Syndrome 11
C16.131.077.272 De Lange Syndrome 4
C16.131.077.299 Deaf-Blind Disorders 65
C16.131.077.313 Donohue Syndrome 1
C16.131.077.327 Down Syndrome 510
C16.131.077.350 Ectodermal Dysplasia 33
C16.131.077.371 Fraser Syndrome 2
C16.131.077.393 Gardner Syndrome 21
C16.131.077.401 Heterotaxy Syndrome 7
C16.131.077.410 Holoprosencephaly 9
C16.131.077.445 Incontinentia Pigmenti 19
C16.131.077.477 Isolated Noncompaction of the Ventricular Myocardium 11
C16.131.077.509 Laurence-Moon Syndrome 6
C16.131.077.525 LEOPARD Syndrome 11
C16.131.077.537 Loeys-Dietz Syndrome 7
C16.131.077.550 Marfan Syndrome 105
C16.131.077.578 Mobius Syndrome 10
C16.131.077.592 Monilethrix 1
C16.131.077.606 Nail-Patella Syndrome 8
C16.131.077.619 Netherton Syndrome 2
C16.131.077.633 Nevus, Sebaceous of Jadassohn 7
C16.131.077.662 Oculocerebrorenal Syndrome 9
C16.131.077.676 Orofaciodigital Syndromes 7
C16.131.077.690 Pallister-Hall Syndrome
C16.131.077.696 Pentalogy of Cantrell 1
C16.131.077.703 POEMS Syndrome 35
C16.131.077.717 Polycystic Kidney Diseases 83
C16.131.077.730 Prader-Willi Syndrome 92
C16.131.077.735 Prolidase Deficiency
C16.131.077.740 Proteus Syndrome 8
C16.131.077.745 Prune Belly Syndrome 3
C16.131.077.790 Rubella Syndrome, Congenital 20
C16.131.077.804 Rubinstein-Taybi Syndrome 12
C16.131.077.850 Short Rib-Polydactyly Syndrome 3
C16.131.077.855 Silver-Russell Syndrome 3
C16.131.077.860 Smith-Lemli-Opitz Syndrome 30
C16.131.077.879 Smith-Magenis Syndrome 2
C16.131.077.889 Sotos Syndrome 4
C16.131.077.899 Trichothiodystrophy Syndromes 1
C16.131.077.919 Trisomy 13 Syndrome 6
C16.131.077.929 Trisomy 18 Syndrome 5
C16.131.077.938 Waardenburg Syndrome 10
C16.131.077.941 Weill-Marchesani Syndrome 1
C16.131.077.944 Wolf-Hirschhorn Syndrome
C16.131.077.970 Zellweger Syndrome 10
C16.131.621 Musculoskeletal Abnormalities 107
C16.131.621.585 Limb Deformities, Congenital 126
C16.131.621.585.174 Arachnodactyly 17
C16.131.621.585.262 Brachydactyly 4
C16.131.621.585.350 Ectromelia 23
C16.131.621.585.512 Lower Extremity Deformities, Congenital 56
C16.131.621.585.600 Polydactyly 31
C16.131.621.585.620 Proteus Syndrome 8
C16.131.621.585.800 Syndactyly 24
C16.131.621.585.984 Thanatophoric Dysplasia 7
C16.131.621.585.988 Upper Extremity Deformities, Congenital 14

Macrocephaly mesodermal hamartoma spectrum Disease MeSH Browser

Add