Mucopolysaccharidosis - Wikipedia, the free encyclopedia 

Mucopolysaccharidosis, Articles lacking sources from December 2007, Articles with unsourced statements since December 2007, Mucopolysaccharidoses, Autosomal recessive, BioMarin Pharmaceutical, Bone, Cartilage, Cell (biology), Connective tissue, Cornea"

Cholesteatoma 

Cholesteatoma - This lesion is somewhat inappropriately named as it is not exactly a tumour nor is it made of cholesterol but rather it is a 3-dimensional collection of epidermal and connective tissues within the middle ear. Its significance lies in the fact that it grows independently and can be locally invasive and destructive. This (usually) unilateral lesion can give rise to a spectrum of problems ranging from painless otorrhoea (discharge from the ear) through to serious central nervous system complications. cholesteatoma, ear, eustachian, conductive hearing loss, deafness, deaf, hearing loss, otorrhoea, vertigo, tympanic membrane perforation, ent, ent., physical examination, examination, facial nerve palsy, facial nerve, symptoms and signs, history, history of, signs

Myositis - Wikipedia, the free encyclopedia 

Myositis, Diseases of the musculoskeletal system and connective tissue, Congenital malformations and deformations of musculoskeletal system, Achilles tendinitis, Adhesive capsulitis of shoulder, Aneurysmal bone cyst, Ankylosing spondylitis, Arteritis, Arthralgia, Arthritis, Arthropathy"

Stickler Syndrome Outreach - Oregon 

This Web site was created at www.homestead.com. You can easily build a customized Web site for yourself or your business using our simple Web page building tools. Oregon Stickler Syndrome connective tissue disorders

Marfan Syndrome Causes, Diagnosis, Symptoms, and Treatment on MedicineNet.com 

Read about Marfan syndrome, a hereditary condition affecting connective tissue. A person with Marfan syndrome may exhibit the following symptoms and characteristics: dislocation of one or both lenses of the eye; a protruding or indented breastbone; scoliosis; flat feet; aortic dilatation; dural ectasia; stretch marks; hernia; and lung collapse. Though there is no cure for Marfan syndrome, there are treatments that can minimize and sometimes prevent some complications. Marfan syndrome, causes, diagnosis, symptoms, treatment, characteristics, signs, Marfan, connective tissue disorder, connective tissue disease, inherited disease, genetic disorder, inherited defect, genetic disease, inherited disorder, genetic defect, affect, cure

Achondroplasia - Wikipedia, the free encyclopedia 

Achondroplasia, Congenital malformations and deformations of musculoskeletal system, Diseases of the musculoskeletal system and connective tissue, 2007, 2008, Abdominal wall defect, Acheiropodia, Achondrogenesis, Amelia (birth defect), Antley-Bixler syndrome, Arachnodactyly"

Epidermolysis bullosa simplex - Genetics Home Reference 

epidermolysis bullosa simplex, Epidermolysis Bullosa, Skin Abnormalities, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Skin Diseases, Genetic, Genetic Diseases, Inborn, Skin Diseases, Skin and Connective Tissue Diseases, Skin Diseases, Vesiculobullous, Epidermolysis Bullosa Simplex, Skin, hair, and nails, EBS-DM, EBS-K, EBS-MP, EBS-WC, hepatiform, KRT14, KRT14 gene, KRT5, KRT5 gene, PLEC1, PLEC1 gene, Epidermolysis Bullosa Simplex Generalized, Epidermolysis Bullosa Simplex Localized, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine

Scoliosis - Wikipedia, the free encyclopedia 

Scoliosis, Articles needing additional references from November 2007, Articles with unsourced statements since April 2007, Articles with unsourced statements since August 2007, Articles with unsourced statements since March 2008, Articles with unsourced statements since January 2008, Diseases of the musculoskeletal system and connective tissue, Fact, Congenital malformations and deformations of musculoskeletal system, 2005, Abdominal cavity"

Osteomyelitis - Wikipedia, the free encyclopedia 

Osteomyelitis, Diseases of the musculoskeletal system and connective tissue, Congenital malformations and deformations of musculoskeletal system, 2006, 2007, 2008, Achilles tendinitis, Adhesive capsulitis of shoulder, Anaerobe, Aneurysmal bone cyst, Ankylosing spondylitis"

Achondroplasia - Wikipedia, the free encyclopedia 

Achondroplasia, Congenital malformations and deformations of musculoskeletal system, Diseases of the musculoskeletal system and connective tissue, 2007, 2008, Abdominal wall defect, Acheiropodia, Achondrogenesis, Amelia (birth defect), Antley-Bixler syndrome, Arachnodactyly"

Ankylosing spondylitis - Wikipedia, the free encyclopedia 

Ankylosing spondylitis, Articles with unsourced statements since June 2008, Diseases of the musculoskeletal system and connective tissue, Congenital malformations and deformations of musculoskeletal system, 2007, 2008, Achilles tendinitis, Acupuncture, Ada Choi, Adalimumab, Adhesive capsulitis of shoulder"

Pneumothorax - Virtual Medical Centre 

Information on the symptoms, treatment and diagnosis of Pneumothorax by professional health specialists." The pleura, connective tissue, lungs, chest cavity, Pneumothorax, lung disease, trauma, tension Pneumothorax"

Asbestosis - Virtual Medical Centre 

Asbestosis is a fibrotic disease of the lungs caused by chronic exposure and inhalation of asbestos fibres. Asbestos is mixture of chemicals that occurs naturally as a fibre substance and was widely used in the building industry for insulation, roofing and fireproofing. Asbestosis damages the connective tissue in the lungs, causing the lungs to become fibrous and stiff. Asbestos exposure can lead to other diseases such as mesothelioma and lung cancer." asbestosis, asbestos, asbestosis symptoms, mesothelioma, asbestos exposure, asbestos symptoms, what is asbestos, asbestos disease, lung disease, asbestos cancer, chrysotile asbestos, asbestos treatment, asbestos poisoning, asbestos diseases, asbestos types, asbestos information, causes, diagnosis, treatment, signs"

Sprains and strains 

Sprains and strains, Sprains and strains are usually minor injuries that often result from sports, exercise, or other physical activity. Sprains refer to an injury to a ligament (the connective tissue that links bones together at joints). Sprains happen most often in the ankle, knee, elbow, or wrist. Strains are tears in muscle tissue. They happen most often in the muscles that support the calf, thigh, groin, and shoulder. Sometimes sprains and strains can be severe, needing weeks of rehabilitation." Sprains and strains"

Niemann-Pick disease - Genetics Home Reference 

Niemann-Pick disease, Sphingolipidoses, Lysosomal Storage Diseases, Nervous System, Brain Diseases, Metabolic, Inborn, Brain Diseases, Metabolic, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases, Histiocytosis, Non-Langerhans-Cell, Histiocytosis, Reticuloendotheliosis, Lymphatic Diseases, Hemic and Lymphatic Diseases, Metabolism, Inborn Errors, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lipoidosis, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Metabolic Diseases, Nutritional and Metabolic Diseases, Niemann-Pick Diseases, Bones, muscles, and connective tissues, Brain and nervous system, Digestive system, Lungs and breathing, lipid metabolism disorder, lysosomal storage disease, lysosomal storage disorder, NPC1, NPC1 gene, NPC2, NPC2 gene, SMPD1, SMPD1 gene, Classical Niemann-Pick Disease, DAF syndrome, lipoid histiocytosis (classical phosphatide), Neuronal Cholesterol Lipidosis, NPD, Ophthalmoplegia Supraoptic Vertical, Sphingomyelinase deficiency

Trisomy 18 - Genetics Home Reference 

trisomy 18, Trisomy, Aneuploidy, Chromosome Aberrations, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Mutation, Variation (Genetics), Genetic Phenomena, Ploidies, trisomy 18, Bones, muscles, and connective tissues, Brain and nervous system, Eyes and vision, Heart and circulation, Lungs and breathing, Chromosomal imbalance syndrome pair 18 trisomy, Complete trisomy 18 syndrome, E3 Trisomy, Edwards Syndrome, Trisomy 16-18, Trisomy 18 syndrome, Trisomy E syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital

Treacher Collins syndrome - wikidoc 

Treacher Collins syndrome, Congenital malformations and deformations of musculoskeletal system, Diseases of the musculoskeletal system and connective tissue, Abdominal wall defect, Acheiropodia, Achondrogenesis, Achondroplasia, Airway, Amelia (birth defect), Antley-Bixler syndrome, Arthrogryposis"

Treacher Collins syndrome - Genetics Home Reference 

Treacher Collins syndrome, Craniofacial Dysostosis, Dysostoses, Bone Diseases, Developmental, Bone Diseases, Musculoskeletal Diseases, Craniofacial Abnormalities, Musculoskeletal Abnormalities, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Mandibulofacial Dysostosis, Bones, muscles, and connective tissues, Ear, nose, and throat, Eyes and vision, Mouth and teeth, TCOF1, TCOF1 gene, Franceschetti-Zwahlen-Klein syndrome, Mandibulofacial dysostosis (MFD1), Treacher Collins-Franceschetti syndrome, zygoauromandibular dysplasia, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history

Treacher Collins syndrome - Wikipedia, the free encyclopedia 

Treacher Collins syndrome, Congenital malformations and deformations of musculoskeletal system, Diseases of the musculoskeletal system and connective tissue, Abdominal wall defect, Acheiropodia, Achondrogenesis, Achondroplasia, Airway, Amelia (birth defect), Antley-Bixler syndrome, Arachnodactyly"

Stickler syndrome - Wikipedia, the free encyclopedia 

Stickler syndrome, Arthritis, Audiology, Autosomal dominant, COL11A1, COL11A2, COL2A1, Cleft palate, Collagen, Collagenopathy, types II and XI, Connective tissue"

Stickler syndrome - Genetics Home Reference 

Stickler syndrome, Collagen Diseases, Connective Tissue Diseases, Skin and Connective Tissue Diseases, Stickler syndrome, Bones, muscles, and connective tissues, Ear, nose, and throat, Eyes and vision, Mouth and teeth, collagenopathy, Hereditary progressive arthro-ophthalmopathy, Stickler syndrome, beaded vitreous type, Stickler syndrome, COL11A1, Stickler syndrome, COL11A2, Stickler syndrome, COL2A1, Stickler syndrome, membranous vitreous type, Stickler syndrome, nonocular type, Stickler syndrome, type 1, Stickler syndrome, type 2, Stickler syndrome, type 3, COL11A1, COL11A1 gene, COL11A2, COL11A2 gene, COL2A1, COL2A1 gene, hereditary arthro-ophthalmo-dystrophy, Hereditary arthro-ophthalmopathy, Stickler dysplasia, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine

Smith-Magenis syndrome - Genetics Home Reference 

Smith-Magenis syndrome, Abnormalities, Multiple, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Smith-Magenis syndrome, Bones, muscles, and connective tissues, Brain and nervous system, Mental health and behavior, contiguous gene deletion syndrome, del 17p11.2, del(17)(p11.2), microdeletion, RAI1, RAI1 gene, chromosome 17p deletion syndrome, deletion 17p syndrome, 17p11.2 monosomy, partial monosomy 17p, SMS, 17p- syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital, heritable disorders, inherited disorders

Shwachman-Diamond syndrome - Genetics Home Reference 

Shwachman-Diamond syndrome, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Shwachman-Diamond syndrome, Bones, muscles, and connective tissues, Food, nutrition, and metabolism, exocrine pancreas deficiency, metaphyseal dysostosis, SBDS, SBDS gene, Congenital Lipomatosis of Pancreas, Metaphyseal chondrodysplasia Shwachman type, SDS, Shwachman-Bodian-Diamond syndrome, Shwachman-Bodian syndrome, Shwachman-Diamond-Oski Syndrome, Shwachman syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital

Rubinstein-Taybi syndrome - Genetics Home Reference 

Rubinstein-Taybi syndrome, Dysostoses, Bone Diseases, Developmental, Bone Diseases, Musculoskeletal Diseases, Craniofacial Abnormalities, Musculoskeletal Abnormalities, Mental Retardation, Neurobehavioral Manifestations, Neurologic Manifestations, Nervous System Diseases, Abnormalities, Multiple, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Chromosome Disorders, Genetic Diseases, Inborn, Rubinstein-Taybi Syndrome, Bones, muscles, and connective tissues, Brain and nervous system, Cancers, Eyes and vision, Heart and circulation, Kidneys and urinary system, Mouth and teeth, 16p13.3 deletion syndrome, contiguous gene syndrome, CREBBP, CREBBP gene, EP300, EP300 gene, Broad Thumb-Hallux Syndrome, RSTS, RTS, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health

Hutchinson-Gilford progeria syndrome - Genetics Home Reference 

Hutchinson-Gilford progeria syndrome, Metabolism, Inborn Errors, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Metabolic Diseases, Nutritional and Metabolic Diseases, Progeria, Bones, muscles, and connective tissues, Food, nutrition, and metabolism, Heart and circulation, Skin, hair, and nails, laminopathy, progeroid, LMNA, LMNA gene, HGPS, Hutchinson-Gilford Syndrome, Progeria, Progeria of childhood, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine, Disease and Gene Association, congenital, heritable disorders, inherited disorders

Osteogenesis Imperfecta: Bone and Connective Tissue Disorders in Children: Merck Man 

Osteogenesis imperfecta - Genetics Home Reference 

osteogenesis imperfecta, Osteochondrodysplasias, Bone Diseases, Developmental, Bone Diseases, Musculoskeletal Diseases, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Collagen Diseases, Connective Tissue Diseases, Skin and Connective Tissue Diseases, Osteogenesis Imperfecta, Bones, muscles, and connective tissues, Ear, nose, and throat, Eyes and vision, Fragilitas ossium congenita, Osteogenesis imperfecta congenita, Osteogenesis imperfecta letalis, Osteogenesis imperfecta tarda, Osteogenesis imperfecta Vrolik type, Osteogenesis imperfecta with normal sclerae, Osteopsathyrosis idiopathica, Trias fragilitis ossium, Van der Hoeve syndrome, wormian bones, COL1A1, COL1A1 gene, COL1A2, COL1A2 gene, CRTAP, CRTAP gene, LEPRE1, LEPRE1 gene, Brittle bone disease, Fragilitas ossium, OI, Vrolik disease, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders

Osteogenesis imperfecta - Wikipedia, the free encyclopedia 

Osteogenesis imperfecta, Articles with unsourced statements since June 2008, Articles with dead external links since March 2008, Congenital malformations and deformations of musculoskeletal system, Diseases of the musculoskeletal system and connective tissue, 2007, Abdominal wall defect, Acheiropodia, Achondrogenesis, Achondroplasia, Alendronate"

Niemann-Pick disease - Genetics Home Reference 

Niemann-Pick disease, Sphingolipidoses, Lysosomal Storage Diseases, Nervous System, Brain Diseases, Metabolic, Inborn, Brain Diseases, Metabolic, Brain Diseases, Central Nervous System Diseases, Nervous System Diseases, Histiocytosis, Non-Langerhans-Cell, Histiocytosis, Reticuloendotheliosis, Lymphatic Diseases, Hemic and Lymphatic Diseases, Metabolism, Inborn Errors, Genetic Diseases, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Lipoidosis, Lipid Metabolism, Inborn Errors, Lysosomal Storage Diseases, Metabolic Diseases, Nutritional and Metabolic Diseases, Niemann-Pick Diseases, Bones, muscles, and connective tissues, Brain and nervous system, Digestive system, Lungs and breathing, lipid metabolism disorder, lysosomal storage disease, lysosomal storage disorder, NPC1, NPC1 gene, NPC2, NPC2 gene, SMPD1, SMPD1 gene, Classical Niemann-Pick Disease, DAF syndrome, lipoid histiocytosis (classical phosphatide), Neuronal Cholesterol Lipidosis, NPD, Ophthalmoplegia Supraoptic Vertical, Sphingomyelinase deficiency

Nail-patella syndrome - Genetics Home Reference 

nail-patella syndrome, Joint Diseases, Musculoskeletal Diseases, Abnormalities, Multiple, Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, Nail Diseases, Skin Diseases, Skin and Connective Tissue Diseases, Nail-Patella Syndrome, Bones, muscles, and connective tissues, Skin, hair, and nails, LMX1B, LMX1B gene, Fong disease, Hereditary onycho-osteodysplasia, Hereditary Osteo-Onychodysplasias, Osterreicher Syndrome, Pelvic Horn Syndrome, Turner-Kieser Syndrome, National Library of Medicine, NLM, National Institutes of Health, NIH, health problem, health problems, disease, diseases, human genetics, gene, genes, genetic disease, genetic conditions, genetic disorders, medical genetics, genetics education, genetics glossary, gene reference, genetics reference, human genetic health, genomic medicine, molecular medicine, genetic testing, genomic medicine, gene therapy, pharmacogenomics, genetic counseling, counseling, gene testing, genome, hereditary family history, future of medicine