| Document Date: 2014-08-19 23:15:59
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Company Lennox / / / IndustryTerm internet relay user / / MedicalCondition Lennox-Gastaut syndrome/ Lennox syndrome West’s syndrome Polyneuropathies / Cerebral palsy Diplegia Hemiplegia Monoplegia Paraplegia Quadriplegia Tetraplegia ndis.gov / paroxysmal disorders / disease Mucolipidosis III / pseudo / Asperger’s disorder / Krabbe disease / Intellectual disability Global Developmental Delay Autism Spectrum Disorders / progressive hypertrophic interstitial polyneuropathy / lysosomal storage disorders / Progressive infantile poliodystrophy Demyelinating diseases / hereditary spastic paralysis/ L1 syndrome / Progressive bulbar palsy / ectodermal dysplasia/ clefting / Deafness/hearing loss / H-S Hunter syndrome / long term learning disabilities / Kugelberg-Welander disease / disintegrative disorder / Thomsens disease / Alpers disease/ Alpers syndrome / Cri du Chat syndrome Dandy-Walker syndrome DiGeorge syndrome/ 22q11 / muscular atrophy / spinal muscular atrophies / Hallervorden-Spatz syndrome / Permanent blindness / Pervasive Developmental Disorders/Autism Spectrum disorders / sclerosis Williams syndrome Wolf-Hirschhorn syndrome / spastic paraplegias / muscular dystrophy Emery-Dreifuss / Mental Disorders / imperfecta Sjogren Larsson syndrome Diseases / mucopolysaccharidoses / bifida VATER syndrome / GM1 gangliosidosis Hartnup disease Homocystinuria Lowe syndrome/ Oculocerebrorenal syndrome Mannosidosis Menkes disease Mucolipidosis II / I / limb deformities / Congenital muscular dystrophy Congenital myotonia / Hoffmann disease / developmental disorder / spastic paraplegia / Tay-Sachs disease / Pantothenate kinase-associated neurodegeneration / neurological impairment Glycine encephalopathy / degenerative diseases / Dejerine-Sottas disease/ Dejerine-Sottas syndrome / Autism / S Hurler-Scheie syndrome / infection Congenital hypothyroidism Congenital iodine-deficiency syndrome / Niemann-Pick disease / III Morquio syndrome/ MPS IVA Maroteaux-Lamy syndrome / neuropathy Infantile Refsum disease / muscular dystrophy Paramyotonia Congenita Cerebral palsy / Hurler syndrome/MPS1-H Scheie syndrome / greater hearing impairment / movement disorders / Leigh syndrome/ Leigh’s disease / Adrenoleukodystrophy / Cockayne syndrome / Louis-Bar syndrome/ Ataxia-telangiectasia Niemann-Pick disease / aciduria Aspartylglucosaminuria Cerebrotendinous xanthomatosis / Friedrich’s ataxia Hereditary / Pompe disease Sandhoff disease / Schindler disease / Pyruvate dehydrogenase deficiency Sialidosis ndis.gov / disorders / encephalomyelopathy Menkes disease / / MedicalTreatment surgery / Amputations / / Organization VACTERL association / National Relay Service / / Person Cornelia de Lange / / / Position occupational therapist / speech pathologist / clinical psychologist / specialist / optometrist / speech pathologist / a psychologist / Governor / pediatrician / psychiatrist / microcephalic primordial dwarfism/ Harper / nurse / physiotherapist / an occupational therapist / H-S Hunter / audiologist / / Product pseudo / Glycine / /
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Evidence of disability or developmental delay (for children under 7 years of age) What to provide with your child’s access request form? So that we can determine whether your child meets the early intervention or devel