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277 Possible Causes for Lordosis, Poor Feeding

  • Nemaline Myopathy 2

    Muscle weakness may also cause difficulty speaking (dysarthria) and swallowing resulting in feeding difficulties.[] Scoliosis and lordosis pose technical difficulties with regard to regional anesthesia.[] difficulties (feeding techniques and calorie-enriched diets).[]

  • Achondroplasia

    Bony characteristics such as vertebral anomalies, lordosis and lumbar scoliosis, limited mouth opening and cervical spine instability make the administration of anesthesia[] Clinical history is a poor predictor of apnea, and polysomnography should be done [ Carroll et al 1995 ].[] Radiographic examination showed typical findings of achondroplasia, such as disproportionately large skull, shortening of limb segments, and lumbar lordosis.[]

  • Mucopolysaccharidosis

    Acta Neurochir (Wien). 2013 Oct;155(10):1973-6. doi: 10.1007/s00701-013-1831-9. Epub 2013 Aug 6. Author information 1 Craniofacial Unit, Department of Pediatric Neurosurgery, Hôpital Universitaire Necker-Enfants Malades, APHP, 149 Rue de Sèvres, 75015, Paris, France, [email protected] Abstract[…][]

  • Congenital Generalized Lipodystrophy Type 4

    Neuromuscul Disord. 2013 May;23(5):441-4. doi: 10.1016/j.nmd.2013.02.005. Epub 2013 Mar 13. Author information 1 Department of Pediatrics, Dokkyo Medical University, Koshigaya Hospital, Koshigaya, Saitama, Japan. [email protected] Abstract A boy with congenital generalized lipodystrophy type 4 with muscular[…][]

  • Congenital Muscular Dystrophy Type 1C

    Affected infants may also develop respiratory and feeding difficulties.[] Clinical features include weakness of the hip and shoulder girdle, difficulty walking, spinal abnormalities including scoliosis, lordosis and kyphosis, and cardiomyopathy.[] The common life-threatening complications of MDC1A include respiratory failure and feeding difficulties.[]

  • Autosomal Recessive Centronuclear Myopathy

    Abstract Centronuclear myopathies (CNM) describe a group of rare muscle diseases typically presenting an abnormal positioning of nuclei in muscle fibers. To date, three genes are known to be associated to a classical CNM phenotype. The X-linked neonatal form (XLCNM) is due to mutations in MTM1 and involves a[…][]

  • Osteoporosis

    This is followed by a loss of lumbar lordosis.[] Other complications include hypercalcemia, irritability, poor feeding, failure to thrive, hypotonia, and more rarely vitamin B 6 -dependent seizures (see Management ).[] (dowager hump) Subsequent loss of lumbar lordosis A decrease in height of 2-3 cm after each vertebral compression fracture and progressive kyphosis Patients with hip fractures[]

  • Multicore Myopathy

    […] congenital-onset facial and neck weakness, slowly progressive severe limb girdle and axial myopathy, respiratory weakness, cardiomyopathy, progressive joint contractures, lumbar lordosis[] […] with external ophthalmoplegia * Neonatal hypotonia * Delayed motor development * Muscle weakness * Amyotrophy * Paralysis of external eye muscles * High arched palate * Poor[] Genitourinary External Genitalia Male: hypogonadotropic hypogonadism Endocrine Features: hypogonadotropic hypogonadism Head And Neck Face: facial weakness Skeletal Spine: lumbar lordosis[]

  • Mucopolysaccharidosis 6

    In patients with the most severe forms of the disease there is a shortened trunk, protuberant abdomen and prominent lumbar lordosis (excessive inward curvature of the lower[] A short trunk with lumbar lordosis is typically present. Corneal opacities can be detected with slitlamp examination.[] A short trunk with lumbar lordosis is typically present.[]

  • Distal Spinal Muscular Atrophy Type 3

    -Postural compensations, Trendelenburg, increased lumbar lordosis -Contractures; usually in the PF's if any less common than in DMD -Scoliosis - Degree depends on ambulation[] difficulties, failure to thrive, respiratory distress, and hearing loss.[] feeding, weak cry, progressive severe hypotonia and weakness affecting limbs and respiratory muscles 2 years without ventilator support SMA-2 ( 20% of cases) 6-18 months[]

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