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Nume Synostosis
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Boli A-Z 3mc Syndrome 49,xxxxy Syndrome Achondroplasia Aging Alagille Syndrome 1 Alport Syndrome, X-Linked Al-Raqad Syndrome Aniridia 1 Anorexia Nervosa 1 Antley-Bixler Syndrome Anus, Imperforate Apert Syndrome Aplasia Cutis Congenita Arthritis Arthrochalasia Ehlers-Danlos Syndrome Astigmatism Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus Azoospermia Beare-Stevenson Cutis Gyrata Syndrome Blepharophimosis Blood Group--Ahonen Blood Group, I System Bone Development Disease Cardiospondylocarpofacial Syndrome Cervicitis Chiari Malformation Chromosomal Triplication Chromosome 2q35 Duplication Syndrome Cocaine Antenatal Exposure Cohen Syndrome Compartment Syndrome Congenital Pseudoarthrosis Congenital Pseudoarthrosis of the Fibula Congenital Radioulnar Synostosis Coronal Synostosis, Syndactyly and Jejunal Atresia Craniofacial Dyssynostosis with Short Stature Craniofacial Microsomia Craniofrontonasal Syndrome Craniosynostosis Crouzon Syndrome Der Kaloustian Mcintosh Silver Syndrome Dysostosis Dysphagia Ear Malformation Esophageal Atresia Fanconi Anemia, Complementation Group E Fetal Alcohol Syndrome Fibular Hypoplasia and Complex Brachydactyly Gillessen-Kaesbach-Nishimura Syndrome Glaucoma-Related Pigment Dispersion Syndrome Greig Cephalopolysyndactyly Syndrome Head Injury Humeroradial Synostosis Humeroradioulnar Synostosis Humero-Ulnar Synostosis Hydrocephalus Hydromyelia Hydronephrosis Hyper-Ige Recurrent Infection Syndrome, Autosomal Dominant Hyper Ige Syndrome Hypertelorism Hypertelorism, Microtia, Facial Clefting Syndrome Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy Hypertropia Hypochondroplasia Hypogonadism Hypogonadotropic Hypogonadism Hypogonadotropism Hypospadias Hypotonia Immunoglobulin E Concentration, Serum Intracranial Hypertension Ischemic Optic Neuropathy Isolated Brachycephaly Isolated Plagiocephaly Isolated Scaphocephaly Jackson-Weiss Syndrome Jejunal Atresia Jorgenson Lenz Syndrome Kienbock's Disease Klippel-Feil Syndrome Lacrimoauriculodentodigital Syndrome Lambdoid Synostosis Lubinsky Syndrome Luteoma Mesomelia Microcephaly Mononeuropathy Muenke Syndrome Multiple Synostoses Syndrome 1 Myositis Myositis Ossificans Neuropathy Opitz Gbbb Syndrome, Type I Osteochondroma Osteoglophonic Dysplasia Parietal Foramina Periostitis Pfeiffer Syndrome Phocomelia Plagiocephaly Polydactyly Polykaryocytosis Inducer Proximal Symphalangism Pseudoarthrosis Ptosis Radial Ray Deficiency, X-Linked Radioulnar Synostosis Radio-Ulnar Synostosis-Amegakaryocytic Thrombocytopenia Syndrome Radioulnar Synostosis-Microcephaly-Scoliosis Syndrome Radioulnar Synostosis, Radial Ray Abnormalities, and Severe Malformations in the Male Radioulnar Synostosis with Microcephaly, Short Stature, Scoliosis, and Mental Retardation Ramer Ladda Syndrome Retinitis Rickets Roberts Syndrome Saethre-Chotzen Syndrome Samson Gardner Syndrome Scoliosis Sensorineural Hearing Loss Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis Simpson-Golabi-Behmel Syndrome Sleep Apnea Spondylocarpotarsal Synostosis Syndrome Spondylocostal Dysostosis 1, Autosomal Recessive Spondyloocular Syndrome Strabismus Synostoses, Tarsal, Carpal, and Digital Synovial Chondromatosis Syringomyelia Tarsal Coalition Tenosynovitis Thoracic Outlet Syndrome Thrombocytopenia Thyroiditis Tibio-Fibular Synostosis Torticollis Ulnar Hypoplasia Williams-Beuren Syndrome