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Træk
Waddling gait
Weakness of the hip girdle and upper thigh muscles, for instance in myopathies, leads to an instability of the pelvis on standing and walking. If the muscles extending the hip joint are affected, the posture in that joint becomes flexed and lumbar lordosis increases. The patients usually have difficulties standing up from a sitting position. Due to weakness in the gluteus medius muscle, the hip on the side of the swinging leg drops with each step (referred to as Trendelenburg sign). The gait appears waddling. The patients frequently attempt to counteract the dropping of the hip on the swinging side by bending the trunk towards the side which is in the stance phase (in the German language literature this is referred to as Duchenne sign). Similar gait patterns can be caused by orthopedic conditions when the origin and the insertion site of the gluteus medius muscle are closer to each other than normal, for instance due to a posttraumatic elevation of the trochanter or pseudarthrosis of the femoral neck.
Resumé
- Også kaldet
- Waddling walk
- Kropssystem
- Abnormality of the nervous system
Waddling gaitHP:0002515
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Bestil min Genome Test129 gener knyttet til Waddling gait
Ændringer i disse gener forårsager sjældne tilstande, hvor Waddling gait ses. De fleste med dette træk har ingen af disse tilstande, og et gen på denne liste siger intet om nogens eget genom.
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| ACBD5acyl-CoA binding domain containing 5 | Altid | I 1 tilstand |
| BGNbiglycan | Altid | I 1 tilstand |
| BICD2BICD cargo adaptor 2 | Altid | I 2 tilstande |
| CCN2cellular communication network factor 2 | Altid | I 1 tilstand |
| COL10A1collagen type X alpha 1 chain | Altid | I 2 tilstande |
| COL2A1collagen type II alpha 1 chain | Altid | I 5 tilstande |
| DMDdystrophin | Altid | I 2 tilstande |
| DPM3dolichyl-phosphate mannosyltransferase subunit 3, regulatory | Altid | I 1 tilstand |
| DYMdymeclin | Altid | I 2 tilstande |
| DYNC1H1dynein cytoplasmic 1 heavy chain 1 | Altid | I 2 tilstande |
| FDX2ferredoxin 2 | Altid | I 1 tilstand |
| FEM1Bfem-1 homolog B | Altid | I 1 tilstand |
| FKBP14FKBP prolyl isomerase 14 | Altid | I 1 tilstand |
| GALNSgalactosamine (N-acetyl)-6-sulfatase | Altid | I 1 tilstand |
| HACD13-hydroxyacyl-CoA dehydratase 1 | Altid | I 1 tilstand |
| HSPB8heat shock protein family B (small) member 8 | Altid | I 1 tilstand |
| LMNAlamin A/C | Altid | I 3 tilstande |
| MBTPS1membrane bound transcription factor peptidase, site 1 | Altid | I 1 tilstand |
| MYH2myosin heavy chain 2 | Altid | I 1 tilstand |
| PHEXphosphate regulating endopeptidase X-linked | Altid | I 1 tilstand |
| PREPLprolyl endopeptidase like | Altid | I 1 tilstand |
| TRIM63tripartite motif containing 63 | Altid | I 1 tilstand |
| TUBA4Atubulin alpha 4a | Altid | I 1 tilstand |
| UFSP2UFM1 specific peptidase 2 | Altid | I 1 tilstand |
| ACTA1actin alpha 1, skeletal muscle | Meget ofte (80–99 %) | I 5 tilstande |
| CCN6cellular communication network factor 6 | Meget ofte (80–99 %) | I 2 tilstande |
| CHST3carbohydrate sulfotransferase 3 | Meget ofte (80–99 %) | I 2 tilstande |
| HNRNPA1heterogeneous nuclear ribonucleoprotein A1 | Meget ofte (80–99 %) | I 1 tilstand |
| HNRNPA2B1heterogeneous nuclear ribonucleoprotein A2/B1 | Meget ofte (80–99 %) | I 1 tilstand |
| LTBP4latent transforming growth factor beta binding protein 4 | Meget ofte (80–99 %) | I 1 tilstand |
| MATN3matrilin 3 | Meget ofte (80–99 %) | I 2 tilstande |
| TRIM32tripartite motif containing 32 | Meget ofte (80–99 %) | I 2 tilstande |
| VCPvalosin containing protein | Meget ofte (80–99 %) | I 1 tilstand |
| ANO5anoctamin 5 | Ofte (30–79 %) | I 1 tilstand |
| AP4B1adaptor related protein complex 4 subunit beta 1 | Ofte (30–79 %) | I 2 tilstande |
| AP4E1adaptor related protein complex 4 subunit epsilon 1 | Ofte (30–79 %) | I 1 tilstand |
| AP4M1adaptor related protein complex 4 subunit mu 1 | Ofte (30–79 %) | I 1 tilstand |
| AP4S1adaptor related protein complex 4 subunit sigma 1 | Ofte (30–79 %) | I 1 tilstand |
| ARHGAP19Rho GTPase activating protein 19 | Ofte (30–79 %) | I 1 tilstand |
| BIN1bridging integrator 1 | Ofte (30–79 %) | I 2 tilstande |
Vis 89 gener mere
| Gen | Hvor ofte det ses | Tilstande |
|---|---|---|
| CFL2cofilin 2 | Ofte (30–79 %) | I 2 tilstande |
| COL13A1collagen type XIII alpha 1 chain | Ofte (30–79 %) | I 1 tilstand |
| COLQcollagen like tail subunit of asymmetric acetylcholinesterase | Ofte (30–79 %) | I 1 tilstand |
| COMPcartilage oligomeric matrix protein | Ofte (30–79 %) | I 4 tilstande |
| DAG1dystroglycan 1 | Ofte (30–79 %) | I 1 tilstand |
| DNAJB6DnaJ heat shock protein family (Hsp40) member B6 | Ofte (30–79 %) | I 1 tilstand |
| DSTYKdual serine/threonine and tyrosine protein kinase | Ofte (30–79 %) | I 1 tilstand |
| EMDemerin | Ofte (30–79 %) | I 2 tilstande |
| FHL1four and a half LIM domains 1 | Ofte (30–79 %) | I 3 tilstande |
| FKRPfukutin related protein | Ofte (30–79 %) | I 2 tilstande |
| GFPT1glutamine--fructose-6-phosphate transaminase 1 | Ofte (30–79 %) | I 2 tilstande |
| HACE1HECT domain and ankyrin repeat containing E3 ubiquitin protein ligase 1 | Ofte (30–79 %) | I 2 tilstande |
| HSPG2heparan sulfate proteoglycan 2 | Ofte (30–79 %) | I 1 tilstand |
| LAMB2laminin subunit beta 2 | Ofte (30–79 %) | I 1 tilstand |
| LRP5LDL receptor related protein 5 | Ofte (30–79 %) | I 1 tilstand |
| MUSKmuscle associated receptor tyrosine kinase | Ofte (30–79 %) | I 1 tilstand |
| MYPNmyopalladin | Ofte (30–79 %) | I 2 tilstande |
| POMT1protein O-mannosyltransferase 1 | Ofte (30–79 %) | I 1 tilstand |
| PTH1Rparathyroid hormone 1 receptor | Ofte (30–79 %) | I 2 tilstande |
| RYR1ryanodine receptor 1 | Ofte (30–79 %) | I 1 tilstand |
| SCN4Asodium voltage-gated channel alpha subunit 4 | Ofte (30–79 %) | I 2 tilstande |
| SGCAsarcoglycan alpha | Ofte (30–79 %) | I 1 tilstand |
| SGCBsarcoglycan beta | Ofte (30–79 %) | I 1 tilstand |
| SGCGsarcoglycan gamma | Ofte (30–79 %) | I 1 tilstand |
| SLC26A2solute carrier family 26 member 2 | Ofte (30–79 %) | I 1 tilstand |
| SLC6A17solute carrier family 6 member 17 | Ofte (30–79 %) | I 2 tilstande |
| SMN1survival of motor neuron 1, telomeric | Ofte (30–79 %) | I 1 tilstand |
| SPEGstriated muscle enriched protein kinase | Ofte (30–79 %) | I 1 tilstand |
| SYNE1spectrin repeat containing nuclear envelope protein 1 | Ofte (30–79 %) | I 1 tilstand |
| SYNE2spectrin repeat containing nuclear envelope protein 2 | Ofte (30–79 %) | I 1 tilstand |
| SYT2synaptotagmin 2 | Ofte (30–79 %) | I 1 tilstand |
| TGFB1transforming growth factor beta 1 | Ofte (30–79 %) | I 2 tilstande |
| TMEM43transmembrane protein 43 | Ofte (30–79 %) | I 1 tilstand |
| TNNC2troponin C2, fast skeletal type | Ofte (30–79 %) | I 1 tilstand |
| TNNT1troponin T1, slow skeletal type | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC10trafficking protein particle complex subunit 10 | Ofte (30–79 %) | I 1 tilstand |
| TRAPPC11trafficking protein particle complex subunit 11 | Ofte (30–79 %) | I 2 tilstande |
| TRPV4transient receptor potential cation channel subfamily V member 4 | Ofte (30–79 %) | I 2 tilstande |
| TTNtitin | Ofte (30–79 %) | I 1 tilstand |
| ALG14ALG14 UDP-N-acetylglucosaminyltransferase subunit | Nogle gange (5–29 %) | I 1 tilstand |
| ALG2ALG2 alpha-1,3/1,6-mannosyltransferase | Nogle gange (5–29 %) | I 2 tilstande |
| ASAH1N-acylsphingosine amidohydrolase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| COL12A1collagen type XII alpha 1 chain | Nogle gange (5–29 %) | I 1 tilstand |
| COL6A1collagen type VI alpha 1 chain | Nogle gange (5–29 %) | I 1 tilstand |
| COL6A2collagen type VI alpha 2 chain | Nogle gange (5–29 %) | I 1 tilstand |
| COL6A3collagen type VI alpha 3 chain | Nogle gange (5–29 %) | I 1 tilstand |
| COL9A1collagen type IX alpha 1 chain | Nogle gange (5–29 %) | I 1 tilstand |
| COL9A2collagen type IX alpha 2 chain | Nogle gange (5–29 %) | I 2 tilstande |
| COL9A3collagen type IX alpha 3 chain | Nogle gange (5–29 %) | I 1 tilstand |
| DEAF1DEAF1 transcription factor | Nogle gange (5–29 %) | I 1 tilstand |
| DPAGT1dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 | Nogle gange (5–29 %) | I 1 tilstand |
| GMPPBGDP-mannose pyrophosphorylase B | Nogle gange (5–29 %) | I 1 tilstand |
| IDH1isocitrate dehydrogenase (NADP(+)) 1 | Nogle gange (5–29 %) | I 1 tilstand |
| KBTBD13kelch repeat and BTB domain containing 13 | Nogle gange (5–29 %) | I 1 tilstand |
| KLHL41kelch like family member 41 | Nogle gange (5–29 %) | I 2 tilstande |
| LAMA2laminin subunit alpha 2 | Nogle gange (5–29 %) | I 1 tilstand |
| LMOD3leiomodin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| MAP3K20mitogen-activated protein kinase kinase kinase 20 | Nogle gange (5–29 %) | I 1 tilstand |
| MYH7myosin heavy chain 7 | Nogle gange (5–29 %) | I 1 tilstand |
| NEBnebulin | Nogle gange (5–29 %) | I 3 tilstande |
| NOGnoggin | Nogle gange (5–29 %) | I 1 tilstand |
| POGZpogo transposable element derived with ZNF domain | Nogle gange (5–29 %) | I 1 tilstand |
| SELENONselenoprotein N | Nogle gange (5–29 %) | I 1 tilstand |
| SLC34A1solute carrier family 34 member 1 | Nogle gange (5–29 %) | I 1 tilstand |
| SLC34A3solute carrier family 34 member 3 | Nogle gange (5–29 %) | I 1 tilstand |
| SPG7SPG7 matrix AAA peptidase subunit, paraplegin | Nogle gange (5–29 %) | I 1 tilstand |
| TPM2tropomyosin 2 | Nogle gange (5–29 %) | I 3 tilstande |
| TPM3tropomyosin 3 | Nogle gange (5–29 %) | I 1 tilstand |
| TTI1TELO2 interacting protein 1 | Nogle gange (5–29 %) | I 1 tilstand |
| VAPBVAMP associated protein B and C | Nogle gange (5–29 %) | I 1 tilstand |
| YY1YY1 transcription factor | Nogle gange (5–29 %) | I 2 tilstande |
| MORC2MORC family CW-type zinc finger 2 | Sjældent (1–4%) | I 1 tilstand |
| ACANaggrecan | Ikke registreret | I 1 tilstand |
| ALPLalkaline phosphatase, biomineralization associated | Ikke registreret | I 1 tilstand |
| CANT1calcium activated nucleotidase 1 | Ikke registreret | I 1 tilstand |
| CHKBcholine kinase beta | Ikke registreret | I 1 tilstand |
| DOK7docking protein 7 | Ikke registreret | I 1 tilstand |
| FGD4FYVE, RhoGEF and PH domain containing 4 | Ikke registreret | I 1 tilstand |
| FLNCfilamin C | Ikke registreret | I 1 tilstand |
| FN1fibronectin 1 | Ikke registreret | I 1 tilstand |
| IFIH1interferon induced with helicase C domain 1 | Ikke registreret | I 1 tilstand |
| MMP13matrix metallopeptidase 13 | Ikke registreret | I 2 tilstande |
| NEFHneurofilament heavy chain | Ikke registreret | I 1 tilstand |
| NEFLneurofilament light chain | Ikke registreret | I 1 tilstand |
| PLEKHG5pleckstrin homology and RhoGEF domain containing G5 | Ikke registreret | I 1 tilstand |
| POC1APOC1 centriolar protein A | Ikke registreret | I 1 tilstand |
| SLC39A13solute carrier family 39 member 13 | Ikke registreret | I 1 tilstand |
| SMARCAL1SNF2 related chromatin remodeling annealing helicase 1 | Ikke registreret | I 1 tilstand |
| TGFB2transforming growth factor beta 2 | Ikke registreret | I 1 tilstand |
Hvor hyppigt det ses hos personer med en af genets tilstande, den hyppigste værdi på tværs af dem, sådan som Human Phenotype Ontology registrerer det. Disse sider beskriver egenskaber og den forskning, der ligger bag dem. De er ikke en diagnose, og hvis du har spørgsmål om symptomer, bør du spørge en læge eller genetisk rådgiver.
Bredere træk
Hvor oplysningerne kommer fra
- Human Phenotype Ontology, udgivelse 2026-09-01: egenskaben, dens navne, definition og de gener, der er knyttet til den. Læs mere på hpo.jax.org.
- Dataudgivelse 2026.10.16-c6eea6bf.
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