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1,071 Possible Causes for Ehlers Danlos Syndrome Classic Type, Spina Bifida

  • Osteoporosis

    Children with health issues such as spina bifida, diabetes, Crohn's disease, and cerebral palsy are at a greater risk for bone disease and can particularly benefit from the[moveforwardpt.com] Ulrich, who lives with multiple disorders, including fibromuscular dysplasia (FMD) and Ehlers-Danlos Syndrome ...[inspire.com] ., Ehlers-Danlos syndrome, vascular type or Ehlers-Danlos syndrome, periodontal type VIII [OMIM 130080 ]) or associated with neutropenia (e.g., ELANE -related neutropenia[ncbi.nlm.nih.gov]

  • Scoliosis

    Neuromuscular scoliosis is associated with a neuromuscular condition such as cerebral palsy , myopathy or spina bifida .[childrenshospital.org] Neuromuscular scoliosis may be a result of other preexisting neuromuscular diseases such as Ehlers-Danlos syndrome, Marfan syndrome, neurofibromatosis, etc.[symptoma.com] Other causes for scoliosis include cerebral palsy, spina bifida, muscular dystrophy, spinal muscular atrophy, and tumors.[medtronic.com]

  • Lethal Occipital Encephalocele - Skeletal Dysplasia Syndrome

    bifida cystica (apperta) -May occur anywhere but lumbar most common -Variable in size and content Spina bifida cystica (apperta) flatting of frontal bones dislocated cerebellium[quizlet.com] syndrome with platelet dysfunction from fibronectin abnormality Ehlers-Danlos syndrome, arthrochalasic type Ehlers-Danlos syndrome, classic type Ehlers-Danlos syndrome, dermatosparaxis[bioreference.net] Thieme, Stuttgart Google Scholar Minns R (1986) The management of children with spina bifida and associated hydrocephalus.[doi.org]

  • Arnold-Chiari Malformation Type 2

    ) (recurrent) 553.9 Hydrancephaly 742.3 with spina bifida (see also Spina bifida) 741.0 Hydranencephaly 742.3 with spina bifida (see also Spina bifida) 741.0 Hydrocephalus[icd9data.com] Results The diagnostic criteria for EhlersDanlos syndrome and related HDCT were met in 357 (12.7%) of the 2813 cases.[doi.org] […] morphometric analyses suggesting a diminished posterior fossa leading to CM-I. 13 , 48 Finally, associations with disorders such as cystic fibrosis, 39 Pierre-Robin syndrome, 28 Ehlers-Danlos[doi.org]

  • Arnold Chiari Malformation

    ) (recurrent) 553.9 Hydrancephaly 742.3 with spina bifida (see also Spina bifida) 741.0 Hydranencephaly 742.3 with spina bifida (see also Spina bifida) 741.0 Hydrocephalus[icd9data.com] Results The diagnostic criteria for EhlersDanlos syndrome and related HDCT were met in 357 (12.7%) of the 2813 cases.[doi.org] The last 3 patients had posttraumatic headache; the second and third patients had limited features of Ehlers-Danlos syndrome (EDS).[ncbi.nlm.nih.gov]

  • Isolated Klippel-Feil Syndrome

    bifida ; Sprengel anomaly ; Ventricular septal defect ; Webbed neck Associated Genes GDF6 (Withdrawn symbols: BMP13, KFS, KFS1, SGM1 ) , MEOX1 (Withdrawn symbols: MOX1 )[mousephenotype.org] […] heterotopia Ehlers-Danlos syndrome type 1 Ehlers-Danlos syndrome, classic type Ehlers-Danlos syndrome, hypermobility type Ehlers-Danlos syndrome, kyphoscoliotic and deafness[sanfordresearch.org] Fact 9: Other associated abnormalities of KFS syndrome are: scoliosis, cleft palate, Duane Syndrome, spina bifida, and heart malformations.[infomory.com]

  • Arnold-Chiari Malformation Type I

    This is usually only seen in children born with spina bifida . Spina bifida is the incomplete development of the spinal cord and/or its protective covering.[webmd.com] There is a probable association between Chiari Malformation and Ehlers-Danlos syndrome ii.[hypermobility.org] Occurs in 90% of patients with myelomeningocele (spina bifida) and is exclusive to this population.[csfinfo.org]

  • Hypermobility Syndrome

    bifida occulta, spondylolisthesis, pectus excavatum or carinatus, prominent lower ribs, etc.[reumatologia-dr-bravo.cl] For more information on specific types from NIH, also check out: • Ehlers-Danlos Syndrome, Classic TypeEhlers-Danlos Syndrome, Hypermobility Type • Ehlers-Danlos Syndrome[edsinfo.wordpress.com] ., spina bifida), diastematomyelia, and tethered cord syndrome may also cause such abnormalities.[ssa.gov]

  • Ehlers-Danlos Syndrome Type Progeroid

    bifida occulta Ambiguous genitalia Gait disturbance Bicornuate uterus Mitral valve prolapse Arthralgia Arteriosclerosis Narrow palpebral fissure Abnormal globe morphology[mendelian.co] Syndrome, Cardiac Valvular Form EHLERS-DANLOS SYNDROME, CLASSIC-LIKE, 2 EHLERS-DANLOS SYNDROME, KYPHOSCOLIOTIC TYPE, 2 Ehlers-Danlos Syndrome, Musculocontractural Type 1[rgd.mcw.edu] AD 40 COL5A1 120215 Ehlers-Danlos syndrome classic type 1 AD 114 COL5A2 120190 Ehlers-Danlos syndrome classic type 2 AD 42 DSE 605942 Ehlers-Danlos syndrome musculocontractural[centogene.com]

  • Ehlers-Danlos Syndrome due to Tenascin-X Deficiency

    bifida occulta 0003298 Stroke 0001297 Percent of people who have these symptoms is not available through HPO Ambiguous genitalia, female Atypical appearance of female genitals[rarediseases.info.nih.gov] ORPHA:230839 Synonym(s): EDS, classic-like type Ehlers-Danlos syndrome, classic-like type Prevalence: Inheritance: Autosomal recessive Age of onset: Neonatal , Childhood ,[orpha.net] My family medical history includes spina bifida, cleft palate, polydactyly, ptosis, pre-term rupture of fetal membrane, gastroesphageal reflux disease, prolapsed mitro valve[mthfrheds.com]

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