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1,945 Possible Causes for Absent Pulp Chambers, Hyperextensible Joints, Osteopenia and Osteoporosis

  • Marfan Syndrome

    Potentially important abnormalities include hyperextensible joints (possible positioning implications), high arched palate (airway implications), pectus excavatum , and kyphoscoliosis[openanesthesia.org] Joint hyperextensibility is present in some, but not all, patients with Marfan syndrome.[dermaamin.com] Sternum deformity—pectus carinatum (outward displacement) or pectus excavatum (inward displacement)—is common, as are joint hyperextensibility (but usually small flexion contractures[merckmanuals.com]

    Missing: Absent Pulp Chambers
  • Autosomal Dominant Hyper-IgE Syndrome

    Nonimmunologic manifestations of HIES include a characteristic face, pathologic dentition, scoliosis, bone alterations, hyperextensible joints, and vascular abnormalities.[ncbi.nlm.nih.gov] Osteopenia or osteoporosis was found in 79% of children and adults.[ncbi.nlm.nih.gov] Common findings among patients were recurrent fractures (in 57 percent of patients), hyperextensible joints (in 68 percent), and scoliosis (in 76 percent of patients 16 years[scienceopen.com]

    Missing: Absent Pulp Chambers
  • Mucopolysaccharidosis

    It is marked by shortness and hyperextension of the neck causing the head to appear as if it were resting directly on the shoulders, short trunk, long extremities with excessive[icd9data.com] Careful positioning and avoidance of hyperextension of the neck are necessary.[medicalhomeportal.org] joint mobility, kyphosis or kyphoscoliosis, pectus carinatum, the sternum extending from clavicular junction and angling downward in midsection, spinal cord compression associated[icd9data.com]

    Missing: Absent Pulp Chambers
  • Ehlers-Danlos Syndrome

    , joint hypermobility and skin fragility to the exceedingly critical consequences of arterial rupture and visceral perforation.[ncbi.nlm.nih.gov] Osteoporosis Pectus excavatum Pectus carinatum Fractures Osteoarthritis Nosebleeds Easy Bruising Hypermobility Scoliosis Poor wound healing Blue sclera TMJ Hypermobility[ctds.info] Ehlers-Danlos syndrome (EDS) is a rare hereditary disorder that results in skin hyperextensibility, joint hypermobility, and tissue fragility.[medcomic.com]

    Missing: Absent Pulp Chambers
  • Singleton Merten Syndrome

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[indjos.com] "[A syndrome of osteogenesis imperfecta, macrocephaly, wormian bones, frontal bossing, brachytelephalangy, hyperextensible joints, congenital blindness and oligophrenia in[wikidoc.org] Abstract Singleton-Merten syndrome (MIM 182250) is an autosomal dominant inherited disorder characterized by early onset periodontitis, root resorption, osteopenia, osteoporosis[ncbi.nlm.nih.gov]

  • Down Syndrome

    hyperextensibility or hyperflexibility Neuromuscular hypotonia Diastasis recti Dry skin Premature aging Congenital heart defects Complications of Down syndrome can involve[emedicine.medscape.com] We provide data on thyroid disease, cervical spine disease, hearing impairment, overweight-obesity, sleep apnea, congenital heart disease, and osteopenia-osteoporosis.[ncbi.nlm.nih.gov] The prevalence of osteopenia ranged from 48% to 52%, and that of osteoporosis ranged from 19% to 22% depending on the site of measurement (femoral neck or lumbar spine, respectively[ncbi.nlm.nih.gov]

    Missing: Absent Pulp Chambers
  • SHORT Syndrome

    Another related syndrome "familial otodentodysplasia" is characterized by the posterior teeth with abnormal morphology, large pulp chambers, short root length compared to[indjos.com] The facial appearance and some of the features resemble the SHORT syndrome, the name being an acronym for Short stature, Hyperextensible joints, Ocular depression, Rieger[ncbi.nlm.nih.gov] ) joints, and a soft out-pouching in the lower abdomen called an inguinal hernia.[ghr.nlm.nih.gov]

    Missing: Osteopenia and Osteoporosis
  • Mucopolysaccharidosis 4A

    […] atlantoaxial joint, requiring limited hyperextension of the neck all of which may complicate laryngoscopy and intubation [ 3 ].[omicsonline.org] In our study, according to BMD assessment by DXA, a half of MPS IVA patients had osteopenia or osteoporosis.[ojrd.biomedcentral.com] It is marked by shortness and hyperextension of the neck causing the head to appear as if it were resting directly on the shoulders, short trunk, long extremities with excessive[icd10data.com]

    Missing: Absent Pulp Chambers
  • Pseudoachondroplasia

    Shortened Limbs Short stubby fingers Waddling walk Joint pain (with age) Large range of joint movement (hyperextensibility) in hands, knees and ankles Limited range of motion[littlepeopleuk.org] […] syndrome with osteopenia 骨減少症を伴う高IgE症候群 Idiopathic juvenile osteoporosis 特発性若年性骨粗しょう症 24.Dysplasias with defective mineralization 24.骨石灰化障害を伴う骨異形成症 Hypophosphatasia-perinatal[normanet.ne.jp] ; an unusually large range of joint movement ( hyperextensibility ) in the hands, knees, and ankles; and a limited range of motion at the elbows and hips.[ghr.nlm.nih.gov]

    Missing: Absent Pulp Chambers
  • Osteogenesis Imperfecta Type 15

    Additional symptoms associated with OI type I include loose (hyperextensible) joints, low muscle tone (hypotonia), and thin skin that bruises easily.[rarediseases.org] […] below peak adult bone mass T-score –1 Osteopenia: BMC or BMD that lies between 1 and 2.5 standard deviations below peak adult bone mass T-score between –1 and –2.5 Osteoporosis[slideshare.net] (hyperextensible) Blue sclera Triangular face Spinal curvature Teeth possibly brittle (dentinogenesis imperfecta) Hearing loss in 20s or 30s Type II Most severe form Usually[en.wikibooks.org]

    Missing: Absent Pulp Chambers

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