Create issue ticket

4,275 Possible Causes for Absent Pulp Chambers, Congenital Heart Disease, Hyperextensible Joints

  • Marfan Syndrome

    Colorado Fetal Care Center Colorectal and Urogenital Care Heart Complex Congenital Heart Disease & Development Clinic Orthopedics Concussion Program Surgery Craniofacial[] Potentially important abnormalities include hyperextensible joints (possible positioning implications), high arched palate (airway implications), pectus excavatum , and kyphoscoliosis[] Joint hyperextensibility is present in some, but not all, patients with Marfan syndrome.[]

    Missing: Absent Pulp Chambers
  • Down Syndrome

    heart disease and Down syndrome.[] hyperextensibility or hyperflexibility Neuromuscular hypotonia Diastasis recti Dry skin Premature aging Congenital heart defects Complications of Down syndrome can involve[] BACKGROUND: The pattern and risk factors for congenital heart diseases (CHD) in children with Down syndrome (DS) vary over time.[]

    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[] Careful positioning and avoidance of hyperextension of the neck are necessary.[] joint mobility, kyphosis or kyphoscoliosis, pectus carinatum, the sternum extending from clavicular junction and angling downward in midsection, spinal cord compression associated[]

    Missing: Absent Pulp Chambers
  • Rubinstein-Taybi Syndrome

    heart disease.[] joints • Small tilted pelvis • Excessive hairiness • Undescended testicles • Feeding difficulties • Respiratory infection • Cardiac anomalies • Vertebral abnormalities •[] Hyperextensible joints were noted. The patient’s thumbs were broad with recently corrected radial angulation.[]

    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[] , SCD/Ventricular Arrhythmias, Atrial Fibrillation/Supraventricular Arrhythmias, Congenital Heart Disease, CHD and Pediatrics and Arrhythmias, CHD and Pediatrics and Prevention[] 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[]

  • Cutis Laxa

    heart disease NGS panel CHD7, ELN, GATA4, GATA6, GDF1, JAG1, NKX2-5, NKX2-6, NOTCH1, NOTCH2, NR2F2, TAB2, TBX1, TBX20, TBX5, ZIC3 Del Dup NGS Connective tissue disorder NGS[] Individuals with these conditions often present with cutis laxa, progeroid features, and hyperextensible joints.[] Other clinical features include hyperelastic skin with easy bruising, varicosities, bladder diverticuli, hernias, hyperextensible joints and multiple skeletal anomalies.[]

    Missing: Absent Pulp Chambers
  • Pierre Robin Syndrome

    Congenital heart disease occurs in about 20 percent of patients with Pierre Robin syndrome.[] They include syndactyly, dysplastic phalanges, polydactyly, clinodactyly, hyperextensible joints, and oligodactyly in the upper limbs.[] There are often signs of congenital heart disease, such as atrial septal defect (ASD), patent ductus arteriosus, ventricular septal defect (VSD).[]

    Missing: Absent Pulp Chambers
  • Noonan Syndrome

    The challenges faced during anesthetic management of patients with NS could be due to congenital heart diseases, hemostatic disorders, and airway anomalies.[] Many affected individuals have hyperextensible joints and muscular hypotonia, albeit the latter generally improves with time.[] An abnormal spinal curvature (scoliosis), hunchback (kyphosis), or clubfoot (talipes equinovarus) is present in 10–15% of patients. 17 Many have hyperextensible joints and[]

    Missing: Absent Pulp Chambers
  • Osteoporosis-Pseudoglioma Syndrome

    Abstract We report a sibship of two brothers and one sister with the osteoporosis-pseudoglioma syndrome and congenital heart disease.[] […] with mutations in LRP5 gene ( low density lipoprotein receptor-related protein-5) Clinical-manifestations short stature osteoporosis spontaneous fractures kyphoscoliosis hyperextensible[] disease.[]

    Missing: Absent Pulp Chambers
  • XXXXY Syndrome

    We have recently seen two patients with the 49,XXXXY syndrome with associated congenital heart disease.[] Other features may include cleft palate, club feet, severely impaired speech, respiratory conditions, behavioral problems, short or broad neck, low birth weight, hyperextensible[] Other features include severely impaired speech, behavioral problems, short or broad neck, low birth weight, hyperextensible joints, short stature, round face in infancy,[]

    Missing: Absent Pulp Chambers

Similar symptoms