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3,600 Possible Causes for Asymmetric Nipples, Average Intelligence, Paraplegia

  • Syringomyelia

    Syringomyelia as a sequel to traumatic paraplegia. Paraplegia. 1981; 19 (2):67–80. [ PubMed ] [ Google Scholar ] Williams B. Progress in syringomyelia.[] A 40-year-old man with complete paraplegia since 1991 as a consequence of a Th4 vertebral fracture showed a great posttraumatic syringomyelia that extended up to C2 vertebral[] […] for rapid progression of curve; - left thoracic scoliosis is common; - treatment of the scoliosis without recognition of syringomyelia and Chiari malformation can lead to paraplegia[]

    Missing: Asymmetric Nipples
  • Amyotrophic Lateral Sclerosis

    The most common form of autosomal recessive hereditary spastic paraplegia is caused by mutations in the SPG11/KIAA1840 gene on chromosome 15q.[] Pathogenic mutations in the KIF5A-SPG10 gene, encoding the kinesin HC5A, can be associated with autosomal dominant hereditary spastic paraplegia (ADHSP).[] Partial paraplegia can be healed by months or sometimes years of physical therapy and other therapies, and developing new rehabilitation techniques is an active field of research[]

    Missing: Asymmetric Nipples
  • Mucopolysaccharidosis

    Morquio A presents average intelligence, and MPS type VI points to deficits partially related to sensory impairment, implying significant differences between them.[]

    Missing: Asymmetric Nipples
  • Mucopolysaccharidosis 4A

    Six new chapters cover congenital myasthenic syndromes, hereditary spastic paraplegia, ion channel disorders, the phakomatoses, beta-galactosidase deficiency, and prion diseases[] On clinical examination, the child appeared to have a less than average intelligence but was placid and cooperative.[] As has been described above, this condition may cause spinal cord compression and paraplegia. Fortunately, this complication is rare.[]

    Missing: Asymmetric Nipples
  • Spinal Muscular Atrophy

    Flaccid paralysis Scoliosis Bed sores: Long term paraplegia may lead to pressure sores Respiratory failure Death Spinal muscular atrophy is transmitted via an autosomal-recessive[] The brain is not affected, and they have been tested to have at least average to above average intelligence.[] Clinically there is a development of paresis over a few days then paraplegia when the abscess is in the lumbar region or quadriplegia when it is located in the cervical area[]

    Missing: Asymmetric Nipples
  • Craniofrontonasal Dysplasia

    "The syndrome of frontonasal dysplasia, spastic paraplegia, mental retardation and blindness: a case report with CT scan findings and review of literature".[] nipples and volume, webbed neck, hand or foot abnormalities such as clinodactyly (most common is a curved 5th finger) and cutaneous syndactyly (webbed fingers / toes).Females[] In conclusion, individuals diagnosed with frontonasal dysplasia usually are of average intelligence and can expect a normal life span.[]

  • X-Linked Spinocerebellar Ataxia Type 5

    ', ‘hereditary spastic paraplegia', ‘epidemiology' and ‘prevalence'.[] paraplegia 35 4 Spastic Paraplegia 39 3 Spastic Paraplegia 4 5 Spastic Paraplegia 42 2 Spastic Paraplegia 43 2 Spastic Paraplegia 44 2 Spastic Paraplegia 45 3 Spastic Paraplegia[] 26(... 781.3 Lack of coordination 334.3 Other cerebellar ataxia 334 Friedreich’s ataxia 334.4 Cerebellar ataxia in diseases classified elsewhere 334.1 Hereditary spastic paraplegia[]

    Missing: Asymmetric Nipples
  • Stuve-Wiedemann Syndrome

    PNPLA6 gene mutations cause hereditary spastic paraplegia (SPG39 HSP), Gordon-Holmes syndrome, Boucher-Neuhäuser syndromes, Laurence-Moon syndrome, and Oliver-McFarlane syndrome[] paraplegia type 15 spastic paraplegia type 2 spastic paraplegia type 31 spastic paraplegia type 3A spastic paraplegia type 4 spastic paraplegia type 7 spastic paraplegia[] ( ) G/A/C coding_sequence_variant, missense_variant, synonymous_variant rs112732576 benign, likely-benign, Spastic paraplegia 39, Mucolipidosis type IV, Spastic Paraplegia[]

    Missing: Asymmetric Nipples
  • Motor Neuron Disease

    Variants in this gene have been found responsible for a recently described form of hereditary spastic paraplegia called SPG49 in two previous reports.[] Patients with hereditary spastic paraplegia or meeting revised El Escorial electrodiagnostic criteria for amyotrophic lateral sclerosis were excluded.[] They include amyotrophic lateral sclerosis (ALS), hereditary spastic paraplegia (HSP), primary lateral sclerosis (PLS), progressive muscular atrophy (PMA), progressive bulbar[]

    Missing: Asymmetric Nipples
  • Parkinson's Disease

    Burnett , Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12 , Human Mutation , 34 , 10 , (1357-1360) , (2013) . P. Zhang, Z. Gao, Y.[] Faculty of Medicine; Executive Director, Office of Ethics, Canadian Medical Association Jeff Blackmer, MD, FRCP(C) is a member of the following medical societies: American Paraplegia[] Battaloglu , PLA2G6 mutations associated with a continuous clinical spectrum from neuroaxonal dystrophy to hereditary spastic paraplegia , Clinical Genetics , 92 , 5 , (534[]

    Missing: Asymmetric Nipples

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