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120 Possible Causes for Hyperextensible Joints, Joint Hypermobility, Lordosis

  • 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[] joint mobility, kyphosis or kyphoscoliosis, pectus carinatum, the sternum extending from clavicular junction and angling downward in midsection, spinal cord compression associated[]

  • Mucopolysaccharidosis 4A

    Ligamentous laxity contributes to joint instability and hypermobility, and may be detrimental in patients suffering from dysplasia of the vertebral column.[] […] atlantoaxial joint, requiring limited hyperextension of the neck all of which may complicate laryngoscopy and intubation [ 3 ].[] In addition, joint hypermobility is unique to MPS IV.[]

  • Hallermann Syndrome

    hypermobility Double-Jointed Flexible joints Increased mobility of joints [ more ] 0001382 Low-set ears Low set ears Lowset ears [ more ] 0000369 Metaphyseal widening Broad[] […] of the joints.[] […] typical 0000752 Hyperlordosis Prominent swayback 0003307 Hypertension 0000822 Hypotrichosis of the scalp Reduced/lack of hair on scalp 0004782 Iris coloboma Cat eye 0000612 Joint[]

  • Pseudoachondroplasia

    […] her rhizomelic dwarfism became increasingly visible, and since completed 15 months of age, when she started to walk, the disease was complicated with genu varum, lumbar lordosis[] Joint hypermobility is seen, especially at the wrists and fingers; however, elbow extension is often limited. Hands and feet are short.[] 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[]

  • Cartilage Hair Hypoplasia

    Increased ligamentous laxity was present in 95%, limited extension of the elbows in 92%, increased lumbar lordosis in 85%, thoracal deformity in 68%, genu varum in 63% and[] All patients have disproportionately short limbs and stature, and most present with skeletal deformities, joint hypermobility, autoimmune deficiency, and anemia.[] Signs and symptoms [ edit ] Short limb dwarfism very fine thin light hairs and eyebrows hyperextensible joints of hand and feet abnormalities of spine neutropenia defective[]

  • Marfan Syndrome

    […] dilatation and dissection , which have historically been the causative factors in early patient demise. [9] Skeletal deformities such as thoracolumbar scoliosis, thoracic lordosis[] Physical examination revealed a lens dislocation with strabismus, high palate, positive wrist and thumb signs, joint hypermobility, and pes planus.[] Potentially important abnormalities include hyperextensible joints (possible positioning implications), high arched palate (airway implications), pectus excavatum , and kyphoscoliosis[]

  • Rubinstein-Taybi Syndrome

    Deformation of internal organs such as cardiac and urinary tract defects is common and so are hyper mobility of joints, funnel chest, scoliosis and lordosis.[] hypermobility, and skin anomalies (in particular keloid formation).[] joints • Small tilted pelvis • Excessive hairiness • Undescended testicles • Feeding difficulties • Respiratory infection • Cardiac anomalies • Vertebral abnormalities •[]

  • Coffin-Lowry Syndrome

    Skeletal anomalies include kyphoscoliosis, lordosis, and pectus carinatum or excavatum. Patients are usually short with delayed bone age; joints are hyperextensible.[] hypermobility syndrome Marshall syndrome Marshall-Smith syndrome Maternal PKU fetal effect Meckel-Gruber syndrome Melnick-Fraser syndrome Menkes kinky-hair syndrome Mental[] joints, muscle atrophy, large and soft hands with simian crease, and tapering of the fingers.[]

  • Stickler Syndrome Type 2

    A bone disease characterized by disproportionate short stature from birth, with a very short trunk and shortened limbs, and skeletal abnormalities including lordosis, scoliosis[] hypermobility Double-Jointed Flexible joints Increased mobility of joints [ more ] 0001382 Long fingers 0100807 Malar flattening Zygomatic flattening 0000272 Micrognathia[] joints * Clubfeet * Prominent large joints * Severe joint disease * Joint pain * Partial dislocation of hip * Spondyloepiphyseal dysplasia * Flat vertebrae * Underdevelopment[]

  • CK Syndrome

    The NSDHL gene encodes 3β-hydroxysteroid dehydrogenase involved in one of the later steps of the cholesterol biosynthetic pathway. Mutations in this gene can cause CHILD syndrome (OMIM 308050) and CK syndrome (OMIM 300831). CHILD syndrome is an X-linked dominant, male lethal disorder caused by mutations in the[…][]

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