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Differential Diagnosis for Delayed speech/language development
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delayed language, Language Delay, Language Delays
Suggest a Missing Condition/DiseaseAvailable only to registered users.
118 possible diagnoses found.
Electromagnetic, Physics, trauma, Radiation Causes
Infectious Disorders (Specific Agent)
Infected organ, Abscesses
Allergic, Collagen, Auto-Immune Disorders
Metabolic, Storage Disorders
- Hurler's mucopolysaccharidosis syndrome
- Kernicterus
- Tay-Sachs disease
- Combined carboxylase/Biotinidase deficiency
- Molybdenum cofactor deficency
- Phenylketonuria/PKU
- Acyl-CoA Dehydrogenase/short chain def
- Cerebral lipidosis disorder
- Krebs cycle/EM cycle metabolic disorder
- LCHAD/Long chain OH-CoA dehydrogenase def
- MCAD/Medium chain OH-CoA Dehydrogenase def
- Proprionic acidemia/congenital
- Succinic Semialdehyde dehydrogenase Deficiency
- VLCHAD/Very Long chain OH-CoA dehydrogenase def
- Alpha-NAGA deficency (Schindler)
- DiFerrente syndrome (Mucopolysaccharidosis VIII)
- Fucosidosis (Anderson-Fabry)
- Histidinemia
- Homocystinuria/homocystinemia
- Hurler-Scheie compound syndrome/mucopol
- Niemann-Pick disease
- Sanfilippo's mucopolysaccharidosis synd
- Tetrahydrobiopterin deficiency/Atypical PKU
- Urea cycle/metabolic disorder
- Barth Syndrome/3 MethylGlutoconic aciduria/MGA II
Deficiency Disorders
Congenital, Developmental Disorders
- Cerebral palsy
- Deafness, congenital
- Down's Syndrome
- Mental retardation
- Asperger syndrome (mild autism)
- CHARGE Congenital syndrome
- Hydrocephalus, obstructive
- Congenital acyanotic heart disease
- Congenital cyanotic heart disease
- Congenital heart disease
- Congenital syndromes
- Cretinism, goitrous sporadic
- Hydrocephalus, communicating
- Ataxic cerebral palsy
- Cretinism
- Infantile autism
- Allan-Herndon Mental Retardation/X-linked
- Encephalopathy, myoclonic, infantile (Kinsbourne)
- Happy puppet syndrome/Angelman syndrome
- Cerebral gigantism of childhood (Sotos)
- Craniocarpotarsal Dystrophy (Freeman Sheldon)
- King Syndrome
- Prader-Willi syndrome
- Robinow dwarfing syndrome/mesomelic dys
- Septo-optic Dysplasia (DeMorsier)
- Silver-Russell syndrome
- Singleton-Merten syndrome
- Velocardiofacial (22q gene) syndrome
- Acro-Facial dysostosis/Nager type
- Brachydactyly Mental Retardation syndrome (2q37)
- Curry-Jones Syndrome
- Foix-Chavany-Marie Syndrome
- Grebe Syndrome
- Hydrocephalus
- Tongue tied/congenital
Hereditary, Familial, Genetic Disorders
- Ataxia-telangiectasia
- Duchenne's Muscular Dystrophy/Pseudohypertrophic
- Fragile X syndrome/X-linked retardation
- Infantile neuroaxonal dystrophy
- Myoclonic encephalopathy/childhood
- Nephritis, hereditary (Alports)
- Tuberous Sclerosis
- Chromosome 22q13.3 deletion syndrome (22q13.3)
- Juberg Marsidi Genetic syndrome (unco)
- Timothy Calcium channel anomaly
- MELAS Encephalopathy
- Pallister W Syndrome
- Dominant SCA/Spinal Cerebellar ataxias
- Cerebellar ataxia, congenital/hered.
- Dysautonomia, familial
- Dystonia musculorum deformans
- Hereditary mitochondrial disorder
- SHORT syndrome (Rieger anomaly plus)
- Torsion dystonia, primary/idiopathic
- Adducted thumbs-Mental retardation syndrome
- Brooks syndrome
- Chromosome 20 deletion/Ring syndrome
- Faciocardiorenal Syndrome (Eastman-Bixler)
Relational, Mental, Psychiatric Disorders
Functional, Physiologic Variant Disorders
Vegetative, Autonomic, Endocrine Disorders
Reference to Organ System
Poisoning (Specific Agent)
Organ Poisoning (Intoxication)
External Links Related to Delayed speech/language development
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