Finding out your child has a medical condition and special needs raises many questions for parents and unfortunately for many of us we do not know all the questions to ask or how to succinctly ask these in the limited time we have with our specialists. Thus, we have provided links to medical databases to give you more info on your child's condition. We suggest you use this as a guide and consult your child's specialists for advice and answers specific to your child.
Click on the letter that your child's medical condition begins with and you will be hyperlinked to medical databases. If your child's condition is not listed follow the hyperlink as it is likely to be on the medical database and contact us at info@specialaussies.com with add (condition name) to A-z medical in the subject line and we will add this to conditions listed.
To find resources and support agencies to support you and your child, please follow the link to our Directory of Services A-Z, which includes associations, support groups, financial assistance, carers and more.
A B C D E F G H I J K L M N O P Q R S T U V W-Z
W-Z
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Acidosis
Acoustic Trauma (Ear Injury)
Acrocephalosyndactyly (Apert Syndrome)
Acquired Immune Deficiency Syndrome (AIDS)
ADD see Attention Deficit Hyperactivity Disorder (ADHD)
ADHD Attention Deficit Hyperactivity Disorder
Adjustment Disorder
Adolescence
Adolescent Depression
Albinism
Allergies
Alport Syndrome
Anaphylaxis
Androgen Insensitivity Synedrome
Anencephaly
Angelman Syndrome
Angelman's Syndrome
Anorchia
Apnoea
Apraxia
Aphasia
Arachnodactyly
Arias syndrome (type II Crigler-Najjar)
Aspergers Syndrome
Aspiration Pneumonia
Ataxia
Atrial Septal Defect
Autism
Auto-immune Disorders
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Bassen-Kornzweig syndrome
Becker's Muscular Dystrophy (Benign pseudohypertrophic muscular dystrophy)
Bernard-Soulier syndrome (Congenital Platelet Function Defects)
Bipolar Disorder
Bleeding Disorders
Blindness
Bloch-Sulzberger syndrome (Incontinentia pigmenti)
Brain Injury
Brain Tumor
Burns
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Canavan Disease
Cancer
Celiac Disease
Cellulitis
Cerebral Palsy
Chediak-Higashi syndrome
Childhood Disintegrative Disorder
Chondroectodermal dysplasia (Ellis-van Creveld syndrome)
Charcot-Marie-Tooth disease
Chylomicronemia Syndrome
Cleft Palate
Club Foot
Congenital Platelet Function Defects
Congential Hip Dysplasia
Cornelia de Lange syndrome
Crigler-Najjar syndrome
Cretinism (Neonatal Hypothyroidism)
Creutzfeldt-Jakob disease
Cri du chat syndrome
Crohn's Disease
Cystic Fibrosis
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Deafness (Hearing Impairment)
Delayed Growth
Delayed milestones, motor and mental development
Depression
Dermatitis
Developmental Dysplasia of the Hip
Diabetes
Down's Syndrome
Drooling
Duchenne Muscular Dystrophy
Dwarfism
Dysphagia
Dystonia
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Ear Injury
Ehlers-Danlos syndrome
Ellis-van Creveld syndrome
Encephalitis
Epilepsy
Expressive Language Disorder
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Failure to Thrive
Familial lipoprotein lipase deficiency
Familial dysautonomia (Riley-Day Syndrome)
Fanconi Syndrome
Fetal Alcohol Syndrome
Fontanelle disorders
Fragile X syndrome
Fructose Intolerance
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Galactosemia
Gastroesophageal reflux
Gaucher disease (Glucocerebrosidase deficiency)
Genetic Disorders
Gigantism
Gilles de la Tourette syndrome
Glanzmann's Disease
Glioma
Glue Ear
Glutaric aciduria and organic acidemias
Glycogen storage disease type V (McArdle syndrome)
Gonadal Dysgenesis (Turner Syndrome)
Gonadal mosaicism
Gorlin's syndrome (Nevoid Basal Cell Carcinoma Syndrome)
Granulomatous ileocolitis (Crohn's Disease)
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Hallerman-Streiff syndrome
Hammer Toe
Hansen's Disease (Leprosy)
Hartnup Disorder
Hearing Impairment
Heller Syndrome (Childhood Disintegrative Disorder)
Hemiplegia
Hemochromatosis
Hemophilia
Hepatitis
Hodgekin's Lymphoma
Huntington's Disease (Chorea)
Hurler Syndrome
Hunter Syndrome
Hutchinson-Gilford syndrome
Hydrocephalus
Hyperglycaemia
Hypoglycaemia
Hypoplastic left heart syndrome
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Impaired Swallowing
Incontinence
Incontinentia pigmenti
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Jaundice
Juvenile Diabetes
Juvenile Rheumatoid Arthritis
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Kidney Disease
Klinefelter Syndrome
Klumpke Paralysis
Kyphosis
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Language Disorder
Legg-Calve-Perthes disease
Leopard Syndrome (Multiple lentigines syndrome)
Leprosy (Hansen's Disease)
Leukaemia
Lock Jaw (Tetanus)
Lou Gehrig's Disease (Amyotrophic lateral sclerosis)
Louis Barr Syndrome (Ataxia-telangiectasia)
Lupus
Lyme Disease
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McArdle syndrome
Marfin Syndrome
Martin-Bell syndrome; Marker X syndrome (see Fragile X syndrome)
Meningitis
Menkes Syndrome
Mental & motor retardation
Metabolic Disorders
Metachromatic Leukodystrophy
Microcephaly
Micrognathia
Mitochondrial Respiratory Chain Disorder
Morquio syndrome
Mucopolysaccharidosis
Multiple lentigines syndrome
Multiple Sclerosis
Muscular Dystrophy
Myasthenia Gravis
Myotonic dystrophy
Myotonia congenita
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Neonatal hypothyroidism
Neuroglioma
Nevoid Basal Cell Carcinoma Syndrome (Gorlin's syndrome)
Niemann-Pick disease
Noonan syndrome
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Obsessive Compulsive Disorder
Olivopontocerebellar atrophy
Opisthotonos
Osler's disease
Osteitis deformans
Osteomalacia
Owren's disease (Factor V Deficiency)
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Paget's Disease
Paralysis
Paramyotonia congenita (Hyperkalemic paralysis)
Paraplegia
Parkinson's Disease
Patau syndrome (Trisomy 13)
Paterson-Kelly syndrome (Plummer-Vinson syndrome/esophageal web)
Pes Cavus
Perthe's Disease
Phonological Disorder
Pierre-Robin Syndrome
PKU
Platelet Function Defect
Polio
Polycythemia
Polysyndactyly
Potter Syndrome
Prader-Willi syndrome
Premature Infant
Progeria
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Quincke's disease
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Rabies
Ramsay Hunt Syndrome
Reifenstein Syndrom
Reflux
Rett Syndrome
Reye Syndrome
Rickets
Right Side Heart Failure
Riley-Day Syndrome
Rubinstein syndrome
Rumination Disorder
Ruptured Eardrum
Russell-Silver Syndrome
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Sanfilippo Syndrome
Scheie Syndrome
Schizophrenia
Scoliosis
Seckel syndrome
Seizure
Shaken Baby Syndrome
Shunt
Sick Sinus Syndrome
Silver-Russell syndrome
SLE
Smith-Lemli-Opitz syndrome
Spasticity
Speech Difficulty
Sphingomyelinase deficiency
Spina Bifida
Spinal muscular atrophy
Spongy degeneration of the brain
Still's disease
Stroke
Stuart-Prower deficiency (Factor X Deficiency)
Stutter
Swallowing Difficulty
Sydenham Chorea
Syndactyly
Syringomyelia
Systemic Lupus Erythmatosus
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Talipes
Tay-Sachs Diesease
Tetanus
Tetralogy of Fallot
Thrombasthenia
Thrombocytopenia
Torticollis
Tourette syndrome
Trisomy 13
Trisomy 18
Trisomy 21
Tuberculosis
Tumor
Turner Syndrome
Type 1 hyperlipoproteinemia
Type 1 glycogen storage disease
Type 1 Diabetes
Typhus
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Ulcerative Colitis
Uncontrolled Muscle Movements
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Valvular pulmonary stenosis
Ventricular Septal Defect
Vision Impairments
Volkmann's contracture
Von Gierke disease
Von Willebrand disease
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Waardenburg-Shah syndrome
Webbing of fingers or toes
Werdnig-Hoffmann Disease
Wermer Syndrome
Williams-Beuren syndrome
Wry Neck