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developmental disorder

see intellectual disability

Related

anomaly development

Specific

agenesis agenesis of the corpus callosum with mental retardation, ocular coloboma & micrognathia amelogenesis imperfecta anhidrotic ectodermal dysplasia ankyloglossia (tongue tie) anophthalmia (microphthalmia 2) anterior chamber cleavage disorder, cerebellar hypoplasia, hypothyroidism aortic supravalvular stenosis aphakia Athabaskan brainstem dysgenesis syndrome (Navajo brainstem syndrome) autosomal dominant aplasia of lacrimal & salivary glands (ALSG) autosomal dominant keratitis autosomal dominant syndactyly; nonsyndromic syndactyly Barth syndrome Bietti's crystalline dystrophy bilateral optic nerve hypoplasia/aplasia Bosley-Salih-Alorainy syndrome bronchopulmonary dysplasia buphthalmos campomelic dysplasia cat-eye syndrome CATCH22 syndrome caudal duplication anomaly cerebro-oculo-facio-skeletal syndrome (COFS); Pena Shokeir 2 syndrome; Cockayne syndrome type 2 CHARGE syndrome coarctation of the aorta congenital alcoholism (teratogenic effects of alcoholism) congenital amegakaryocytic thrombocytopenia congenital anomaly (birth defect) congenital cataracts facial dysmorphism & neuropathy syndrome Cornelia de Lange syndrome Costello syndrome (faciocutaneoskeletal syndrome) craniolenticulosutural dysplasia craniometaphyseal dysplasia cryptophthalmos syndrome (Fraser syndrome) cryptorchidism deafness with labyrinthine aplasia, microtia & microdontia (LAMM) delayed puberty developmental bone disorder developmental delay developmental disorder of aldosterone deficiency developmental disorder syndrome (multisystem disorder) developmental dyspraxia developmental thyroid disease dsytonia deafness syndrome; Mohr-Traneberg syndrome; deafness-dystonia-optic atrophy syndrome; X-linked progressive deafness type 1 Dyggve-Melchior-Clausen syndrome ectopia pupillae enteroptosis; Glenard's disease ethylmalonic encephalopathy familial chronic mucocutaneous candidiasis with thyroid disease (CMCT) familial deafness Farber disease (Farber lipogranulomatosis) fibrous dysplasia focal cortical dysplasia foveal hypoplasia Friedreich ataxia hemiplegia alterans (alternating hemiplegia) hereditary hyperekplexia (Kok disease, startle disease, stiff baby syndrome) heterotaxia; heterotaxy; situs ambiguus hip dysplasia hypoparathyroidism, sensorineural deafness & renal dysplasia (HDR syndrome) hypospadius hypotrichosis-lymphedema-telangiectasia syndrome IGF1 resistance (resistance to insulin-like growth factor 1) imperforate hymen infantile epileptic encephalopathy infantile systemic hyalinosis infundibular hypoplasia & hypopituitarism intellectual disability; mental retardation Jensen syndrome; opticoacoustic nerve atrophy with dementia Johanson-Blizzard syndrome (JBS) juvenile hyaline fibromatosis Legg-Calve-Perthes disease; pseudocoxalgia; avascular necrosis of the hip lethal type multiple pterygium syndrome long face syndrome; skeletal open bite low birth weight infant (preterm infant) lymphedema-hypoparathyroidism syndrome malformation; dysmorphism malrotation of the intestine Meckel syndrome Meckel's diverticulum (ileal diverticulum) metabolic bone disease microglossia microphthalmia (nanophthalmos) Mobius syndrome; congenital facial diplegia; oromandibular-limb hypogenesis Muellerian aplasia multiple synostoses syndrome myoclonic encephalopathy nemaline myopathy (rod myopathy) neurocristopathy nonlethal type multiple pterygium syndrome; Escobar syndrome; Escobar variant multiple pterygium syndrome oral-facial-digital syndrome osteopetrosis (Albers-Schonberg disease) pancreatic agenesis Parry-Romberg syndrome (progressive hemifacial atrophy) pectus carinatum; pigeon breast; keeled chest pectus excavatum Pelizaeus-Merzbacher-like disease pervasive developmental disorder; autism spectrum disorder (ASD) Peters-plus syndrome phenytoin teratogenesis phocomelia pontocerebellar hypoplasia popliteal pterygium syndrome pseudohypoparathyroidism pulmonary hypoplasia pyelectasis (pyelectasia) rhombencephalosynapsis Rubinstein-Taybi syndrome Sabjad-Sakati syndrome; hyoparathyroidism-retardation-dysmorphism (HRD) Schwartz-Jampel syndrome (SJS1) septo-optic dysplasia (de Morsier's syndrome) Shprintzen syndrome; velocardiofacial syndrome slipped femoral epiphysis Smith-Magenis syndrome speech-language disorder; specific language impairment; developmental verbal dyspraxia split-hand/foot malformation stapes ankylosis with broad thumb & toes Sturge-Weber syndrome (encephalotrigeminal angiomatosis) symphalangism proximal syndrome tarsal-carpal coalition syndrome tight hymenal ring tooth agenesis transient erythroblastopenia of childhood VACTERL van der Woude syndrome (lip-pit syndrome) VATER syndrome Warburg micro syndrome Warburg micro syndrome 4 (WARBM4)

General

chronic disease

References

  1. National Institute of Neurological Disorders and Stroke (NINDS) NINDS Pervasive Developmental Disorders Information Page https://www.ninds.nih.gov/disorders/all-disorders/pervasive-developmental-disorders-information-page
  2. Eunice Kennedy Shriver National Institute of Child Health and Human Development Intellectual and Developmental Disabilities (IDDs): Condition Information https://www.nichd.nih.gov/health/topics/idds/conditioninfo/default
  3. [No authors listed] Identifying infants and young children with developmental disorders in the medical home: an algorithm for developmental surveillance and screening. Pediatrics. 2006 Jul;118(1):405-20. PMID: 16818591