Ehlers danlos type 4

Ehlers-Danlos syndromes (EDS) are a group of genetic connective tissue disorders. Symptoms may include loose joints, joint pain, stretchy velvety skin, and abnormal scar formation Ehlers-Danlos syndrome type IV, the vascular type of Ehlers-Danlos syndromes (EDS), is an inherited connective tissue disorder defined by characteristic facial features (acrogeria) in most patients, translucent skin with highly visible subcutaneous vessels on the trunk and lower back, easy bruising.. Ehlers Danlos type 4. 92 likes. A rare genetic connective tissue disorder characterized by small joint hypermobility, easy bruising and characteristic.. Ehlers Danlos syndrome, ecchymotic type; Ehlers Danlos syndrome, arterial type; Ehlers Danlos syndrome, Sack-Barabas type; Ehlers Danlos syndrome Vascular Ehlers-Danlos syndrome is an inherited connective tissue disorder that is caused by defects in a protein called collagen

Ehlers-Danlos syndromes - Wikipedi

(PDF) Ehlers-Danlos syndrome type I

  1. Ehlers-Danlos syndrome type IV: A rare genetic connective tissue disorder characterized by small joint hypermobility, easy bruising and characteristic facial appearance - a vascular or ecchymotic form of the condition. More detailed information about the symptoms, causes, and treatments of Ehlers-Danlos..
  2. Ehlers-Danlos syndrome type VIIA and VIIB result from splice-junction mutations or genomic deletions that involve exon 6 in the COL1A1 and COL1A2 genes Tsipouras P, et al. Ehlers-Danlos syndrome type IV: cosegregation of the phenotype to a COL3A1 allele of type III procollagen. Hum Genet
  3. Research of Ehlers-danlos Syndrome, Type 4 has been linked to Ehlers-danlos Syndrome, Aneurysm, Connective Tissue Diseases Ehlers-danlos Syndrome, Type 4 Bioinformatics Tool. Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes..

Video: Ehlers Danlos type 4 - Home Faceboo

Vascular Ehlers-Danlos syndrome Genetic and Rare Diseases

  1. Several types of Ehlers-Danlos syndromes and treatments are described. Ehlers-Danlos syndromes are a group of disorders which share common features including easy bruising, joint hypermobility (loose joints), skin that stretches easily (skin hyperelasticity or laxity), and weakness of..
  2. ant. Bruisability is a pro
  3. Chain565: Ehlers-Danlos Syndrome, Type IV. « Back to App Chain search. Atelosteogenesis, Type II Epiphyseal Dysplasia 4, Multiple Diastrophic Dysplasia
  4. e University's Pathophysiology of Complex Patient Problems project
  5. The Ehlers-Danlos syndromes (EDS) are a heterogeneous group of heritable connective tissue disorders (HCTDs). There is a huge variation in presentation, impact and severity. Most types of EDS affect joints and skin and most feature joint hypermobility. Additional features vary by type and they..
  6. Ehlers-Danlos syndrome, type IV is the vascular type Ehlers-Danlos syndrome. It results from mutations in the COL3A1 gene
  7. Ehlers-Danlos syndromes (EDS) are a group of rare inherited conditions that affect connective tissue. Connective tissues provide support in skin, tendons, ligaments, blood vessels, internal organs and bones

Ehlers - Danlos syndrome (EDS) is defined as a group of hereditary disorders that affect connective tissues due to a defect in collagen. Many types of EDS share universal symptoms. A common symptom that occurs in most forms of Ehlers - Danlos is hypermobility of the joints Ehlers-Danlos syndrome (EDS) comprises a group of inherited heterogeneous disorders that share a common decrease in the tensile strength and Castori M. Ehlers-Danlos syndrome, hypermobility type: an underdiagnosed hereditary connective tissue disorder with mucocutaneous, articular, and.. Ehlers-Danlos syndrome (all types combined) has been reported as 1 per 5000 to 1 per 10,000 population; however, the exact prevalence and incidence of Ehlers-Danlos type 4 is not exactly known and is considered rare. Unfortunately there are not way to fix your shoulder problem and best advise..

Orphanet: Ehlers Danlos syndrome type 4

  1. Vascular Ehlers-Danlos syndrome (EDS) or type IV Ehlers-Danlos syndrome (EDS 4) is the most malignant form of Ehlers-Danlos syndrome. This form is often accompanied by neurovascular complications secondary to vessel dissections and/or aneurysms
  2. Ehlers-Danlos syndrome (EDS) is an inherited connective tissue disorder with different presentations that have been classified into several primary types. EDS is caused by a defect in the structure, production, or processing of collagen or proteins that interact with collagen..
  3. Ehlers Danlos syndrome (EDS) is a collection of genetic disorders that affect connective tissue. People who have EDS have problems with their collagen, a The specific EDS type most associated with arthritis is hypermobility type (hEDS). This type is known for frequent joint dislocation, degenerative..
  4. Chain565: Ehlers-Danlos Syndrome, Type IV. « Back to App Chain search. Atelosteogenesis, Type II Epiphyseal Dysplasia 4, Multiple Diastrophic Dysplasia
  5. < > We can help. EDS UK is the only UK charity to offer support to people touched by all types of Ehlers-Danlos syndrome. That is why we are here, that is what drives us to work everyday. To offer support to anybody touched by Ehlers-Danlos syndrome

Ehlers-Danlos syndrome (EDS) is a connective tissue disorder that has been classified into several primary types. It is caused by a defect in the structure Ehlers-Danlos syndrome, cardiac valvular form, Osteogenesis imperfecta type 1, Osteogenesis imperfecta type 2, Osteogenesis imperfecta.. Ehlers-Danlos syndrome has specific consequences relating to development of the skeletal system. Since joints are stabilized by cartilage that is partially composed of collagen, individuals with Ehlers-Danlos syndrome often suffer dislocations or sprains of the joints Ehlers-Danlos syndrome. Author: Dr Varitsara Mangkorntongsakul, Senior Medical Officer, Central Coast Local Health District, NSW, Gosford/Hamlyn Terrace, NSW, Australia. Dr Yi Jia Lee, Junior Medical Officer, North Metropolitan Health Service, WA, Perth, Australia. DermNet NZ Editor in Chief.. Ehlers-Danlos syndrome - Wikipedia, the free encyclopedia. Spontaneous liver rupture in EhlersDanlos syndrome type IV. Siew Chien Ng, MRCP and Paolo Muiesan, MD Eh ler sDa n los sy n dr om e t y pe IV ca n esca pe dia g n osis u n t il t h e dev elopm en t of ca t a st r oph ic com plica t.. Ehlers-Danlos syndrome (EDS) consists of a heterogeneous group of disorders which are part of a larger group of connective tissue disorders (also A. P. Barabas, Heterogeneity of the Ehlers-Danlos syndrome: description of three clinical types and a hypothesis to explain the basic defect(s), British..

What are the Ehlers-Danlos Syndromes? The Ehlers Danlos Societ

Ehlers-Danlos syndrome is a group of inherited disorders marked by extremely loose joints, hyperelastic skin that bruises easily, and/or easily damaged blood vessels. It is caused by a genetic mutation in which the body creates less collagen Узнать причину. Закрыть. Ehlers danlos syndrome classical type. The Balesky. Загрузка... Louise's Prolotherapy Story (Ehlers-Danlos Syndrome and Comprehensive Prolotherapy) - Продолжительность: 7:23 Caring Medical Regenerative Medicine Clinics 9 699 просмотров The ehlersdanlos community on Reddit. Reddit gives you the best of the internet in one place. The decision to have children is an extremely personal one, Ehlers Danlos Syndrome or not. In order to avoid further bullying and harassment, it is now against subreddit rules to make comments regarding..

Ehlers-Danlos Syndrome Treatments: Conservative Therapies and SI Joint Surgery EDS has no cure, so no treatment can completely rid you of the disorder. Gazit Y, Jacob G, Grahame R. Ehlers-Danlos Syndrome—Hypermobility Type: A Much Neglected Multisystemic Disorder People with the classical form of Ehlers-Danlos syndrome experience wounds that split open with little bleeding and leave scars that widen over time to Each type of EDS is a distinct disorder that 'runs true' in a family, the Ehlers-Danlos National Foundation says. This means that an individual with.. Discover ideas about Ehlers Danlos Syndrome Types. Ehlers-Danlos Syndrome Type IV: Blue Sclerae. Acupuncture For Migraine - The levator scapulae runs between the upper part of the shoulder blades and the top four cervical vertebrae

síndrome de Ehlers-Danlos (es); Ehlers-Danlos szindróma (hu); Ehlers-Danlos-en sindrome (eu); síndrome d'Ehlers-Danlos (ca) ); Zespół Ehlersa i Danlosa (pl); Елерса — Данлоса синдром (uk); Ehlers Danlos Syndroom, Ehlers danlos type 3 (nl); Elers - Danlos sindromu (az); Sidekudoksien.. Ehlers-Danlos syndrome (EDS) is, unfortunately, a condition you may not know much about unless you (or a close friend) have it. Then a couple of weeks later when I told him I officially had EDS hypermobility type, he said at least we finally know. — Jennifer L Connective Tissue. Ehlers-Danlos Syndrome. Topics. unknown mutation. Vascular - Type IV (vascular). autosomal dominant, rarely autosomal recessive. translucent skin, arterial/intestinal/uterine fragility and spontaneous rupture, extensive bruising Ehlers-Danlos syndrome occurs in several forms. In type IV disease there is a defect in type III collagen synthesis. Which of the following symptoms would be most expected in a patient with this disorder

Ehlers-Danlos Syndrome isn't rare - it's just rarely diagnosed Jan Groh. It took me forty-three and a half years to get a diagnosis of EDS hypermobility type. Ehlers-Danlos Syndrome (EDS) is a genetic connective tissue disorder caused by structural deficiencies in collagen, the most abundant protein in.. The Ehlers-Danlos syndromes (EDS) are heritable connective tissue disorders affecting the quality of collagen in every part of the body. They were once considered to be very rare and only seen by rheumatologists. There are 13 types of Ehlers-Danlos syndrome, most of which are indeed rare Ehlers-Danlos syndrome is a rare genetic disorder that affects connective tissues and results in flexible joints, elastic skin, and fragile tissues. Some types of EDS are characterized by weaknesses in the walls of the hollow organs of the gastrointestinal tract, in the esophagus, the cardiovascular system.. I have Ehlers Danlos Syndrome too!!! However I have type 3, hypermobile. I inherited it from my mothers side of the family and so far just me and her and a cousin show symptoms. I was diagnosed around the age of 4-5. In fact this past November I dislocated both knees due to EDS. I would love to..

Ehlers-Danlos Syndrome Type 4 (EDS Type) - Symptom

Ehlers-Danlos syndrome. classic type (types I/II). vascular type (type IV). kyphoscoliotic form (type VI). Clinical description. Ehlers-Danlos syndrome (EDS) is a clinically heterogeneous connective tissue disorder that can affect the integrity of the skin, joints, blood vessels and internal organs Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders. Inspire. Ehlers-Danlos Syndromes and Hypermobility Spectrum Disorders. I have type 3 with TONS of classical overlap symptoms...I have 6 tatts and had no trouble with any of them...they did take a bit longer to heal, but.. Ehlers-Danlos syndromes (EDS) are a genetically and clinically heterogeneous group of disorders characterized by a fragility of the soft connective tissues [12]. The Villefranche classification recognizes six EDS subtypes among which classical, hypermobility and vascular types are the most frequent.. Molecular pathology COL3A1 mutations occur in Ehlers-Danlos syndrome type IV, and in aortic and arterial aneurysms

Ehlers-Danlos Syndrome. Moises Dominguez. relatively rare. hypermobility Ehlers-Danlos syndrome (EDS) is the most common type Ehlers-Danlos syndromes are a group of genetic connective tissue disorders.[1] Symptoms may include loose joints, joint pain, stretchy skin, and abnormal scar formation.[1] These can be noticed at birth or in early childhood.[2] Complications may include aortic dissection, joint dislocations, scoliosis.. Ehlers-Danlos Syndrome. Books about types of EDS. Score. 1 of 5 stars 2 of 5 stars 3 of 5 stars 4 of 5 stars 5 of 5 stars. 2. A Guide to Living with Ehlers-Danlos Syndrome (Hypermobility Type): Bending without Breaking (2nd edition) by Ehlers-Danlos Syndromes are complex and multisystem diseases with clinical symptoms that vary depending on the type of collagen altered. And although Ehlers-Danlos Syndromes mostly affect the joints and skin, the severity of the defects in the connective tissues range from mild discomfort to..

Ehlers-Danlos Syndrome. Ehlers-Danlos syndromes are a genetically, biochemically, and clinically diverse group of heritable connective tissue disorders. They have joint laxity and dermal features in common


Ehlers-Danlos syndrome type IV Symptoms - RightDiagnosis

#ehlers danlos type 3 #ehlers danlos zebra #ehlers danlos problems #ehlers danlos syndrome #postural orthostatic tachycardia syndrome #dysautonomia #innapropriate sinus tachycardia #fibromyalgia #hypermobility syndrome #sponnie #potsie Ehlers-Danlos Syndrome (EDS) is a rare genetic disorder that affects the body's connective tissues, like the skin, joints, ligaments, and blood vessel walls. There are a number of distinct subtypes of EDS, some dangerous. But, the basic issue is that the body has a problem with collagen production, which..

Ehlers Danlos Syndromes - NORD (National Organization for Rare

Acquired von Willebrand°s syndrome and Ehlers-Danlos syndrome presenting with gastro-intestinal bleeding. Scand J Haematol 1979;22:305-10. Persistent atypical varicella in two renal transplant patients and its relation to mycophenolic acid Sir, Mycophenolic acid (MPA).. Ehlers-Danlos syndrome is a group of genetic disorders that cause loose joints and skin. The condition can also affect tissue, organs, bones and blood vessels. There are 13 types of Ehlers-Danlos syndrome.. Vascular Ehlers-Danlos syndrome: Placing recent studies into context Mitzi L. Murray, MD, MA EDNF Annual Learning Conference August 10, 2012 For me context is the key - from that comes the understanding Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type

The Ehlers-Danlos syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders affecting as many as 1 in 5000 individuals, characterized by [3] classified EDS into six major types (Table 1): classical type (OMIM#130000), hypermobility type (OMIM#130020), vascular type (OMIM#.. Ehlers-Danlos syndrome is a group of genetic connective tissue disorders characterized by unstable, hypermobile joints, loose, stretchy skin, and There are several different types of Ehlers-Danlos syndrome, each with its own set of features and complications. The most common form of.. Ehlers-Danlos' syndrom er den hyppigst forekommende arvelige bindevevssykdommen. Det er en mulig differensialdiagnose til kjente lidelser i muskel- og skjelettsystemet. Symptomene på Ehlers-Danlos' syndrom avhenger av hvilken type av sykdommen man har The vascular type of Ehlers-Danlos syndrome, type IV, is associated with severe complications, including arterial rupture and visceral perforation. However, to our knowledge, there has been only one previous report of splenic rupture caused by a spontaneous hemorrhage in type IV..

Ehlers-Danlos syndrome (EDS) is a group of connective tissue disorders that can occur in families. Learn about EDS and available genetic testing With most types of EDS there is a 50% (1 out of 2) chance that each child of a parent with EDS will also have EDS. Not everyone with EDS is affected.. Ehlers-Danlos: The frequency of ehlers-danlos syndrome (all types) has been reported as 1 per 5000 to 1 per 10, 000 in the population. Type IV can: Ehlers-danlos syndrome is a genetic disorder of the collagen fibers in the body (the stuff that keeps the tissues tough) A severe form of Ehlers-Danlos syndrome, a group of connective tissue disorders characterized by skin hyperextensibility, articular hypermobility, and tissue fragility. EDSVASC is an autosomal dominant disease characterized by joint and dermal manifestations as in other forms of the syndrome, and by.. For Ehlers-Danlos, for all intents and purposes, it is PROCOLLAGEN PEPTIDASE DEFICIENCY. You've gotta know that when the collagen is extruded from For Menkes syndrome (Ehlers-Danlos type-IX), you've gotta know that there's defective COPPER UPTAKE from the intestines

Ehlers-danlos Syndrome, Type 4: Disease Bioinformatics: Novus

Ehlers-Danlos causes connective tissues to be weaker and more elastic. This means that skin may bruise easier or joints may become extremely loose and overly flexible. There are at least ten different types of Ehlers-Danlos, which affect different collagen genes and lead to varying combinations of.. ehlers-danlos.org/. I hope this helps, but perhaps you could speak to your doctor again and s/he might be able to clarify further. Classical Girl. You may also like... Pregnancy and Ehlers Danlos Type 3. welcomed, relating to either condition and the roads you followed. Thanks in advance Vascular variant of Ehlers-Danlos syndrome[edit]. Vascular EDS (formerly categorized as type 4) is identified by skin that is thin, translucent, extremely fragile, and bruises easily. It is also characterized by fragile blood vessels and organs that can easily rupture. Affected people are frequently short, and..

Ehlers Danlos Syndrome (EDS) is a heterogeneous group of heritable connective tissue disorders characterized by joint hypermobility, skin hyperextensibility, cardiac valvular defects and tissue fragility. There are eight major types of EDS (see Table 1), classified according to symptoms and signs Ehlers-Danlos syndrome, type 4: Read more about symptoms, causes, diagnosis, tests, types, drugs, treatments, prevention, and more information. Symptoms of Ehlers-Danlos syndrome, type 4. Clinical features: Imported from Human Phenotype Ontology (HPO) Several types of EDS exist, and the prognosis depends on the type and individual. Treatment, including the use of medical marijuana for Ehlers-Danlos, can help manage symptoms and avoid or minimize complications Ehlers- Danlos Syndrome (EDS). Robert Whittaker, SPT University of North Dakota. Overview. Genetic defects affecting biosynthesis & structure of collagen type (autosomal recessive - AR, autosomal dominant - AD) 2 Slideshow 2124448 by ulric

Beim Ehlers-Danlos-Syndrom handelt es sich um eine seltene Erkrankung. Bei den verschiedenen Formen des Ehlers-Danlos-Syndrom konnten humangenetisch Defekte folgender Gene nachgewiesen werden Ehlers-Danlos Syndrome, Classic Type (inkl Ehlers-Danlos is a disease caused by abnormal collagen synthesis. Different types of Ehlers-Danlos effect different types of collagen. The most common presentation includes stretchy skin, easy bruising, aneurysms (due to weak vessels) & hypermobile joints Ehlers-Danlos syndrome. Welcome to the latest in our series of informational blogs looking at healthcare in general and specific medical conditions in I was diagnosed in my early 20s with type III. Earliest symptoms when I was young were pain with running, joint hypermobility - tricks for friends..

Ehlers-Danlos Syndrome Types & Hypermobility Symptom

Ehlers-Danlos Syndromes are four different disorders characterised by hypermobility and skin which breaks easilyCredit: Getty - Contributor. What's the life expectancy for Ehlers-Danlos Syndrome? Life expectancy depends on the type of EDS. vEDS can be a life shortening illness, because of the.. Ehlers-Danlos Syndrome Test Guide. The Collagen Diagnostic Laboratory offers diagnostic testing for EDS type I and II (classical EDS), EDS type IV (vascular EDS), EDS type VI (kyphoscoliotic EDS), EDS types VIIa and VIIb (arthrochalasia), and EDS type VIII (periodontal EDS). There is presently no.. Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type. (English) Syndrome d'Ehlers Danlos : la présidente de l'association ASED ( apprivoiser les syndromes d'Ehlers-Danlos) témoigne à l'occasion du vernissage d'une exposition de l'ASED, du 11 au 19 décembre 2009 dans la sale du Carré d'Art de Montgeron Heart, 88(IV): 20-28. Pepin M., Schwarze U., Superti-Furga A. et al. (2000) Clinical and genetic features of Ehlers-Danlos syndrome type IV, the vascular type

Ehlers-Danlos syndrome type 4

Ehlers-Danlos syndrome (EDS) is a non-inflammatory, hereditary disease of the connective tissue. Depending on the type of EDS. Some have few ailments and most have normal life expectancy. However, large deformities in the thoracic skeleton are detrimental to the heart and lungs in the long.. collagen type V alpha 1 chain (COL5A1). LOVD v.2.0 Build 36 [ Current LOVD status ] Register as submitter | Log in. View all sequence variants of a certain type. Simple search. Query the database by selecting the most important variables (exon number, type of variant, disease phenotype) — 696 с.; Paolo Narcisi, Allan J.Richards, Stanley D. Ferguson, F.Michael Pope. (1994). A family with Ehlers — Danlos syndrome type III/articular hypermobility syndrome has a glycine 637 to serine substitution in type III collagen

Ehlers-Danlos Syndrome, Type IV Sequencing

One of the most frustrating things about Ehlers-Danlos Syndrome is that it's possible to go through your entire life without ever knowing which 'type' you have. My joints don't regularly dislocate (some started subluxing as I reached my mid-twenties), but by the time I turned 19 I had the kind of pelvic.. Page 1 and 2: Vascular Ehlers Danlos Syndrome (ED. For this magazine there is no download available. Magazine: Vascular Ehlers Danlos Syndrome (EDS type IV. Close What Is Ehlers-Danlos Syndrome? Types of EDS. Causes. Diagnosis. Treatment. Living With EDS. Ehlers-Danlos syndrome (EDS) is a disease that weakens the connective tissues of your body. These are things like tendons and ligaments that hold parts of your body together. EDS can make your joints.. Ehlers-Danlos syndrome (EDS) refers to a group of rare genetic disorders affecting the connective tissue that makes up the skin, joints, and blood vessels Ehlers-Danlos syndrome (EDS) can lead to fatigue and chronic pain for many patients, making it difficult for them to stay motivated to do..

De Vereniging van Ehlers-Danlos patiënten (VED) bestaat sinds 1984. De vereniging is opgericht om mensen die aan EDS lijden te helpen bij al hun vragen Alle activiteiten van de vereniging zijn er op gericht meer bekendheid te geven aan en meer inzicht te krijgen in het syndroom van Ehlers-Danlos Ehlers-Danlos syndromes (EDS) are inherited connective tissue disorders with variable severity; features include skin fragility, joint hypermobility, and rupture of blood Thirteen different types of EDS are currently recognised, with the molecular basis known in all except for hypermobile EDS Case notes from nddc: ehlers-danlos syndrome type IV The Ehlers-Danlos syndrome (EDS) comprises a heterogenous group of nine hereditary connective tissue disorders, characterized by hyperelasticity of Two children born on Crete of consanguinous parents presented the following manifestations of the ocular type of Ehlers-Danlos syndrome (EDS).. A Guide to Living with Ehlers-Danlos Syndrome (Hypermobility Type) by Isobel Knight Paperback £14.99. A Multidisciplinary Approach to Managing Ehlers-Danlos (Type III) - Hypermobility Syndrome: Working With the Chronic Complex Patient Medical definition of Ehlers-Danlos syndrome: an inherited disorder of connective tissue with several clinical forms characterized especially by extremely flexible joints, elastic skin, and Post the Definition of Ehlers-Danlos syndrome to Facebook Share the Definition of Ehlers-Danlos syndrome on Twitter

  • String muuttuja.
  • Kaveri on kateellinen.
  • Kinderkakku iltalehti.
  • Spider man homecoming koko elokuva keskustelu.
  • Energiahoito pori.
  • F1 lyhenne.
  • Arkkitehtuuri kulttuuri.
  • Kiinan kielen alkeet turku.
  • Kunlun red star facebook.
  • Tuomari sarjakuvahahmo elokuvat ja tv ohjelmat.
  • Julma henri al qaida finland youtube.
  • Myydään pesukone turku.
  • Jerseyn hintataso.
  • Lihan savustus pöntössä.
  • Lounas factory.
  • Frozen sähköhammasharja citymarket.
  • Energiahoito rauma.
  • Fazer tuotantotyöntekijä.
  • Hoasin palvelukeskuksesta.
  • Uness progress.
  • Convert to pdf.
  • Mary stuart masterson.
  • Emo abkürzung.
  • Selma vilhunen elokuvat.
  • Orgeat siirappi.
  • Tiketti seppälä.
  • Vanhustenhoito artikkeli.
  • Amazing race season 29 winners.
  • Nyx kulmakynä.
  • Iphone nukkumispainike.
  • Wettervorhersage deutschland 14 tage.
  • Opinnäytetyön loppuseminaari esitys.
  • Ipanema vai waist trainer.
  • Lämmin kanasalaatti.
  • Menuetto takki.
  • Foreo kokemuksia demi.
  • Glykolipidi.
  • Dolce gusto kapselit kierrätys.
  • Kahvikuppi tekstillä.
  • Avantgarde acoustic trio xd.
  • Turskafile pannulla.