| Document Date: 2014-08-19 23:15:23
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Company Lennox / / / IndustryTerm internet relay user / / MedicalCondition mucopolysaccharidoses / bifida VATER syndrome / Sly syndrome / I/ Werdnig Hoffmann disease / disease Mucolipidosis III / pseudo / GM1 gangliosidosis Hartnup disease Homocystinuria Lowe syndrome/ Oculocerebrorenal syndrome Mannosidosis Menkes disease Mucolipidosis II / I / limb deformities / Krabbe disease / progressive hypertrophic interstitial polyneuropathy / lysosomal storage disorders / developmental disorder / Cri du Chat syndrome Dandy-Walker / Speech impairment Permanent blindness / spastic paraplegia / Tay-Sachs disease / Pantothenate kinase-associated neurodegeneration / Intellectual/ learning impairment Intellectual disability Global Developmental Delay Autism Spectrum Disorders / neurological impairment Glycine encephalopathy / degenerative diseases / Angelman syndrome CHARGE syndrome Cockayne syndrome / hereditary spastic paralysis/ L1 syndrome / Progressive infantile poliodystrophy Demyelinating diseases / S Hurler-Scheie syndrome / Progressive bulbar palsy / Niemann-Pick disease / ectodermal dysplasia/ clefting / DiGeorge syndrome / Deafness/hearing loss / III Morquio syndrome/ MPS IVA Maroteaux-Lamy syndrome / long term learning disabilities / muscular dystrophy Paramyotonia Congenita Cerebral palsy / Kugelberg-Welander disease / Hurler syndrome/MPS1-H Scheie syndrome / greater hearing impairment / movement disorders / Thomsens disease / Leigh syndrome/ Leigh’s disease / Tuberous sclerosis Williams syndrome Wolf-Hirschhorn / Alpers disease/ Alpers syndrome / muscular atrophy / spinal muscular atrophies / Hallervorden-Spatz syndrome / Episodic and paroxysmal disorders Lennox-Gastaut syndrome/ Lennox syndrome West’s syndrome Polyneuropathies / muscular dystrophy Congenital myotonia / deficiency / peripheral nervous system Dejerine-Sottas disease/ Dejerine-Sottas syndrome / Louis-Bar syndrome/ Ataxia-telangiectasia Niemann-Pick disease / aciduria Aspartylglucosaminuria Cerebrotendinous xanthomatosis / Pervasive Developmental Disorders/Autism Spectrum disorders / Friedrich’s ataxia Hereditary / Schindler disease / Pompe disease Sandhoff disease / central nervous system Adrenoleukodystrophy / spastic paraplegias / syndrome / Mental Disorders / disorders / muscular dystrophy Emery-Dreifuss / imperfecta Sjogren Larsson syndrome Diseases / / MedicalTreatment Amputations / surgery / / Organization VACTERL association / National Relay Service / / Person Cornelia de Lange / / / Position speech pathologist / a psychologist / Governor / pediatrician / psychiatrist / microcephalic primordial dwarfism/ Harper / nurse / occupational therapist / speech pathologist / clinical psychologist / physiotherapist / an occupational therapist / H-S Hunter / specialist / audiologist / optometrist / / 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 dev