0845 300 1348
Achondroplasia Paraplegia
Acquired Brain Injury
Adrenal Hypoplasia Congenita
Agenesis of the Corpus Callosum
Aicardi Gutieres Syndrome
Aicardi Syndrome
Airway Obstruction
Alcohol Related Neurodevelopmental Delay
Allagille Syndrome
Alpers' Syndrome
Angelman Syndrome
Arnold Chichi Syndrome
Arthogryposis Multiplex Congenita
Aspergers
Asthma
Ataxia Telangiectasia
Ateriovenous Malformation
Atypical Terratoid Rhabdoid Tumour
Autism
Batten Disease
Becker's Muscular Dystrophy
"Bi-lated Haemorragic Retinitis,"
Bilateral below knee amputation
Bilateral lower limb deficiency
Bilateral Periventricular Leucomalacia
Bi-lateral Retinal Detatchment
Bilateral Talipes
Bingham Syndrome
Bladder Extrophy
Branchio Oscilio Syndrome
Bulbar Palsy
C2/3 Spinal Cord Injury
Canavan Disease
Cancer
Cardio-Facio Cutaneous Syndrome
Cavernous Angioma
Cerebellar Ataxia
Cerebellar Atrophy
Cerebellar Hypoplasia
Cerebral Palsy
Charcot Marie Tooth Disease
Charge Syndrome
Chari Malformation
Chromasome 22 Deletion
Chromasome 22 Translocation
Chromasome 22 Trisomy Mosaic
Chromosome 1p Deletion
"Chromosome 4, Trisomy 4P"
Chromsome 17 Micro Deletion
Chronic Chest Disease
Chronic Lung Disease
Chronic Osteomyelitis
Chronic Post Viral Fatigue
Chronic Reflux
Chronic Renal Failiure
CMU resulting in Microcephaly
Cockayne Syndrome
Complex Congenital Heart Defect
Congenial Muscular Dystrophy
Congenital Adrenal Hyperplasia
Congenital Axonal Neuropathy
Congenital Bilateral Perisylvian Polymicrogyria
Congenital Central Hypoventilation Syndrome
Congenital Core Myopathy
Congenital Heart Defect
Congenital Muscular Dystrophy
Congenital Myasthenia
Congenital Myopathy
Congenital Myotonic Dystrophy
Congenital Nemaline Myopathy
Congenital Toxoplamosis
Congenital Tracheo-Oesophageal Fistula
Congential Cataracts
Congential Cortical Dysplasia
Congential Cytomgalovirius
Congential Lymphangiecta
Congential Myasthenic Syndrome
Cornelia de Lange Syndrome
Cortical Vision Impairment
Costello Syndrome
Craniosynostosis
Cri Du Chat Syndrome
Cromosome 14 q Deletion
Cryptogenic Infantile Spasms
Cutis Marmorata Telangiectatica
Cystic Fibrosis
Cystic Periventricular Leukomalacia
Cytomegalovirus
Dandy-Walkers Syndrome
Delayed Development
Delayed Speech
Developmental Delay
Developmental Dyspraxia
Di George Symdrome
Dilated Cardiomyopathy
Dobowitz Syndrome
Double Stroke
Down Syndrome
Dravet's Syndrome
Duchene Muscular Dystrophy
Duplication on chromsome 11q
Dyspraxia
Ehlers-Danlos Syndrome
Encaphalitis
Encysted 4th ventricle
Ependymoma
Eperdermolysis Bullosa Simplex
Epilepsy
Epileptic Encephalopathy
Escabar Syndrome
Facioscapulohumeral Muscular Dystrophy
Fibrodysplasia Ossificans Progressiva
Foetal Alcohol Syndrome
Fragile X Syndrome
Friedreichs Ataxia
Fumerate Hydratase Deficiency
Ganglianeuroma Tumour
Gastro reflux
Genetic Heart Condition
Global Development Delay
Global Learning Delay
Glutaric Aciduria Type 1
Glycogen Storage Disease Type O
Goldenhar Syndrome
Grade 4 Intraventricular Bilateral Haemorrhage
Hemiplegia
Hereditary Muscle Weakness
Hereditary Spastic Paralegia
Histiocytosis X
Hodgkin's Lymphoblastic Lymphoma
Hodgkin's Lymphoma
Homozygote Acute Intermittment Porphgria
Hpoxic Brain Injury
Hunter Disease
Hydrancephaly
Hydrocephalus
Hypomobility of the joints
Hypoplastic Left Heart syndrome
Hypoplastic Right Ventricle
Hypotonia
Hypoxic Ischamic Encephalopathy
Infantile spasms
Intracerebral haemorrhage
Intractable Epilepsy
ip 36.22 Chromosone Deletion
Juvenile Dermatomyositis
Juvenile Enthesitus Related Arthritus
Juvenile Idiopathic Arthritis
Juvenile Parkinsons Disease
Juvenille Huntingtons Disease
Kabuki Syndrome
Kneist Syndrome
Landau Kleffner Syndrome
Langer Giedeon Syndrome Type 2
Laryngealmalacia
"Laryngotrachera Mylacia,"
Late Infantile Battens Disease
Learning Difficulties
Lebers Amauresis Nystagmus
Left Congenital Talipes
Left Hemiplebia
Leigh's Disease
Lennox Gastraut Syndrome
Leukeamia
Leukodystrophy
Limb Dystonia
Limb Girdle Muscular Dystrophy
Linsencaphaley Walker Warburgh Type 2
Lipomeningocele
Lissencaphly
Liver failure
Lung disease
Malignant Glioma in Thalamus
MCADD
McCune Albright Syndrome
Meares-Irlen Syndrome
MELAS Epilepsy
Meningitis
Meningococcal Septicaemia
Mental Health Problems
Metachronmatic Leukodystrophy
Microcephaly
Miller Dieker Syndrome
Minicore Muscular Dystrophy
Minor Atrophy to Cerebellum
Missing Right hand & right leg longer than the left
Mitral Valve Stenosis
Mitrochondrial Disorder
Mono SP1
Monoplygia
Morquio Syndrome
Motor Dyspraxia
Mowatt Wilson Syndrome
MTHFR deficiency
Mucopolysaccharide Storage Disease Type III
Muscular Dystrophy
Myoclonic Epilepsy
Myoclonic Epilepsy
Myofibrillar Myopathy
Myotonic Dystrophy
Myotubular Myopathy
Neimann Pick type C
Nemaline Rod Myopathy
Neurocutaneous Malanosis Sequence
Neuro-degenerative Condition
Neurofibromitosis
Neurological Brain Disease
Neurological Condition
Neuronal Migration Disorder
Niemann - pick type c
Noonan's Syndrome
Nuerofibromatosis type 1
Opitz Trigonocephaly Syndrome
Osteogenesis Imperfecta
Otahara Syndrome
Pachygyria
Pacygyria
Panhypopituitarism
Paralytic Poliomyelites
Paraplegia
Paroxysmal Non-Kinesogenic Choreothetosis
Partial Trisomy 13
Partial Trisomy 14
Partial trisomy 14q
Partial Trisomy of Chromsome 3
Pataw Syndrome
Peadiatric Neurotransmitters Disease
Peho Syndrome
Pelizaeus-Merzbacher Disease
Perisylvianian Syndrome
Periventricular Cysts
Periventricular Leukomalacia
Peter's Anomoly
Phenylketonuria
Plagiocephaly
Polmicogyria
Polycystic Kidneys
Polyostotic fibrous dysplasia
Polystotic Fibrous Displaysia
Ponto Cerebellar Hypoplasia Type 2
Prader-Willi Syndrome
Primary Hyperoxaluria Type I
Profound Deafness
Progeria
Pulmonary Atresia
Pulmonary Hypertension
Pulmonary stenosis
Pyruuate Dehydrogenase
Quadriparesis
Rasmussen's Encaphilitics
Reflux
Renal failiure
Restrictive Cardiomypathy
Retinopathy
Retinopathy of prematurity
Rett's Syndrome.
Right Hemiplegia
Rod Cone Dystrophy
Rubenstein-Taybi Syndrome
San Fellipo Syndrome
Schizencephaly
Semi Lobar Holoprosenchaphaly
Sensory Integration disorder
Septo Optic Dysplasia
Severe Learning Difficulties
Severe Myoclonic Epilepsy
Severe neuro-developmental problem
Sexual Abuse
Shaken Baby Syndrome
Short gut syndrome
Sickle Cell disease
Silver Russell Syndrome
Sleep Apneoa
Spinal Muscular Atrophy Type 2
Spinal Muscular Atrophy Type 3
Sodium Valporate Syndrome
Soto's Syndrome
Spina Bifida
Spinal Astrcytoma
Spondylo Metaphyseal Dysplasia
Static Encephalopathy
Static Encephapy
Sticklers Syndrome
Stroke
Subvalvar Aortic Stenosis
SWAN - Syndrome without a name
Syringomyelia
T2 Paraplegic
Terthering of spinal cord
Tetraplegia
Tourettes syndrome
Tracheostomy
Translocation trisomy 11q - 22q
Tricuspid Atresia
Trisomy 18 q deletion
Trisomy 22
Tuberous Sclerosis
Turner's Syndrome
Udiagnosed Overgrowth Syndrome
Ulrich's Congenital Muscular Dystrophy
Unbalanced Translocation of Chromosome 22 Deletion
Unbalanced Translocation of Chromosome 6 + 11
Vanishing White Matter Disease
Vater Association
Vein of Galen Malformations
Ventricular Septal Defect
Verbal & Motor Dyspraxia
Viral Encephalitis
Visual Impairement
Vulva Crohns Disease
Wager Syndrome
West Sydrome
Wolf Hirschhorn Syndrome
XXXXY Syndrome (49 XXXXY)
