Developmental Disorder: Causes & Reasons

Possible Causes for Developmental Disorder

Developmental and Epileptic Encephalopathy Type 6

KEYWORDS: Cognitive decline; Dravet syndrome; Language developmental disorders [ncbi.nlm.nih.gov]

[…] types, profound to severe developmental delay, and movement disorders. [neurology.org]

disorder with severe speech and ambulation defects ADAM22 Epileptic encephalopathy, early infantile, 61 ADAR Aicardi-Goutieres syndrome 6 ADSL Adenylosuccinase deficiency [asperbio.com]

Fanconi Anemia

FA is a hematological and developmental disorder caused by mutations in more than 20 different genes. [ncbi.nlm.nih.gov]

Cockayne syndrome (CS) is a genetic disorder characterized by developmental abnormalities and photodermatosis resulting from the lack of transcription-coupled nucleotide excision [ncbi.nlm.nih.gov]

Fanconi anemia (FA) is a rare autosomal recessive disorder clinically characterized by developmental abnormalities, progressive bone marrow failure (BMF) and profound cancer [ncbi.nlm.nih.gov]

Duchenne Muscular Dystrophy

Policy Statements and Clinical Reports Motor Delays: Early Identification and Evaluation Identifying Infants and Young Children with Developmental Disorders in the Medical [aap.org]

National Task Force for Early Identification of Childhood Neuromuscular Disorders. Developmental delay, do a CK. [svalovadystrofia.sk]

Home: An Algorithm for Developmental Surveillance and Screening Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays Education [aap.org]

Hypogammaglobulinemia

[…] anomalies Section Eight Metabolic and systemic diseases Section Ten Pigmentary disorders Section Twelve Infections infestations and bites 81 Antimicrobial drugs 403 Volume [books.google.com]

(2018) ., Management of Inherited Bleeding Disorders in Pregnancy, BJOG: An International Journal of Obstetrics & Gynaecology, 124, 8, (e193-e263), (2017). [doi.org]

Because B, T, and natural killer (NK) cells share a common progenitor, defects occurring at early developmental stages may result in combined immunodeficiency involving all [wikidoc.org]

Autism

> # Journal of autism & developmental disorders (Online) schema:name " Journal of autism & developmental disorders (Online) "@ en ;. http://www.worldcat.org/title/-/oclc/321086369 [worldcat.org]

Disorders is the leading peer-reviewed, scholarly periodical focusing on all aspects of autism spectrum disorders and related developmental disabilities. [link.springer.com]

Fombonne E 2005 Epidemiology of autistic disorder and other pervasive developmental disorders. J Clin Psychiatry 66 : 3–8 3. [doi.org]

Asperger Syndrome

Synonyms Aspergers disorder Asperger's disorder Atypical autism Atypical childhood psychoses Borderline psychosis of childhood Developmental disorder, pervasive, active state [icd9data.com]

The disintegrative disorders: Childhood disintegrative disorder and Rett's disorder. In: Psychoses and pervasive developmental disorders in childhood and adolescence. [doi.org]

Developmental dyspraxia is not limited to imitation in children with autism spectrum disorders. [dx.doi.org]

Childhood Schizophrenia

CONCLUSIONS: Findings support the validity of this developmental concept for a multiple complex developmental disorder and give preliminary, "first-cut" validity to these [ncbi.nlm.nih.gov]

In young children this disorder is usually a severe developmental disorder nearly always leading to long term impairment. [online-clinic.com]

[…] and multiple complex developmental disorder. [ncbi.nlm.nih.gov]

Axenfeld-Rieger Syndrome

It is an inheritable developmental disorder with complete penetrance and variable expression [1,2]. [slideshare.net]

Abstract Mutations in the Forkhead Box C1 (FOXC1) transcription factor gene are associated with Axenfeld-Rieger syndrome (ARS), a developmental disorder affecting structures [ncbi.nlm.nih.gov]

Somatic and anterior chamber malformations in this patient represent a developmental disorder of the neural crest. [ncbi.nlm.nih.gov]

Atypical Autism

Pervasive Developmental Disorder Not Otherwise Specified "Pervasive developmental disorder not otherwise specified" (PDD-NOS) is a term used more and more commonly, particularly [mugsy.org]

A pervasive developmental disorder not otherwise specified ( PDD-NOS ) is one of the four autism spectrum disorders (ASD) [1] and also one of the five disorders classified [en.wikipedia.org]

Childhood Disintegrative Disorder Childhood Disintegrative Disorder (CDD) is a Pervasive Developmental Disorder (PDD) which looks almost exactly like autism. [mugsy.org]

Mowat-Wilson Syndrome

Mowat-Wilson syndrome (MWS) is an autosomal dominant developmental disorder with mental retardation and variable multiple congenital abnormalities due to mutations of the [ncbi.nlm.nih.gov]

Definition A complex developmental disorder characterized by mental retardation, delayed motor development, epilepsy, microcephaly and a wide spectrum of clinically heterogeneous [uniprot.org]

OMIM : 56 Mowat-Wilson syndrome is an autosomal dominant complex developmental disorder; individuals with functional null mutations present with mental retardation, delayed [malacards.org]

Cornelia De Lange Syndrome

Abstract Cornelia de Lange syndrome (CdLS, also called Brachmann-de Lange syndrome - BdLS) is a multisystem developmental disorder characterized by distinctive facial features [ncbi.nlm.nih.gov]

Cornelia de Lange Syndrome (CdLS) is a rare developmental disorder that is present from birth. [cdls.org.uk]

Cornelia de Lange syndrome (CdLS) is a developmental disorder which is characterized by typical facial features, upper extremity malformations, and growth and cognitive delays [ncbi.nlm.nih.gov]

Alveolar Capillary Dysplasia

Abstract Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins (ACDMPV) is a developmental disorder of the lungs, primarily affecting their vasculature. [ncbi.nlm.nih.gov]

Abstract Alveolar capillary dysplasia with misalignment of pulmonary veins (ACD/MPV) is an autosomal dominant, fatal developmental disorder of the lungs, with a mortality [ncbi.nlm.nih.gov]

AB - Alveolar capillary dysplasia with misalignment of pulmonary veins (ACDMPV) is a lethal lung developmental disorder caused by heterozygous point mutations or genomic deletion [scholars.northwestern.edu]

Progressive Osseous Heteroplasia

@inproceedings{Macewen2006TwoNC, title={Two new case reports and follow-up of three Progressive osseous heteroplasia : a distinct developmental disorder of}, author={G. [semanticscholar.org]

Progressive osseous heteroplasia is a rare developmental disorder of mesenchymal differentiation characterized by cutaneous osteomas in infancy and by progressive heterotopic [ncbi.nlm.nih.gov]

Abstract Progressive osseous heteroplasia (POH) is a rare developmental disorder of heterotopic ossification (HO) caused by heterozygous inactivating germline mutations in [ncbi.nlm.nih.gov]

Familial Developmental Dysphasia

Familial aggregation of a developmental language disorder. Cognition, 39 (1), pp. 1-50. Gopnik M, Crago MB. Familial Aggregation of a Developmental Language Disorder. [wwww.unboundmedicine.com]

Are Developmental Disorders Like Cases of Adult Brain Damage? [amazon.de]

VOLUME TWO: BEHAVIOURALLY DEFINED DEVELOPMENTAL DISORDERS Does the Autistic Child Have a “Theory of Mind”? [amazon.it]

Developmental Disorder

Many advances have been made in the field of pediatric imaging, particularly with regard to research involving children with developmental disorders. [ncbi.nlm.nih.gov]

Visit the website for Div. 33: Intellectual and Developmental Disabilities/Autism Spectrum Disorder. [apa.org]

Large numbers of people with co-occurring developmental disorders and mental illnesses now live in the community. [ncbi.nlm.nih.gov]

Baraitser-Winter Syndrome

Abstract Baraitser–Winter cerebrofrontofacial syndrome (BWCFF) (BRWS; MIM #243310, 614583) is a rare developmental disorder affecting multiple organ systems. [doi.org]

Abstract Baraitser-Winter Cerebrofrontofacial syndrome (BWCFF) [BRWS; MIM #243310, 614583] is a rare developmental disorder affecting multiple organ systems. [rde.dspace-express.com]

Pilz Published in Clinical genetics 2017 DOI: 10.1111/cge.12864 Baraitser-Winter cerebrofrontofacial syndrome (BWCFF) (BRWS; MIM #243310, 614583) is a rare developmental disorder [semanticscholar.org]

Helsmoortel-van der Aa Syndrome

Deciphering Developmental Disorders S. Prevalence and architecture of de novo mutations in developmental disorders. Nature. 2017;542(7642):433–8. pmid:28135719. [journals.plos.org]

disorder [DS:H00773] Description Helsmoortel-van der Aa syndrome (HVDAS) is an autism spectrum disorder (ASD), accompanied with intellectual disability and facial dysmorphisms [genome.jp]

Am J Med Genet C. 2014; 166: 315-326 Deciphering Developmental Disorders Study Group Largescale discovery of novel genetic causes of developmental disorders. [ejpn-journal.com]

Trevor Disease

Dysplasia epiphysealis hemimelica (DEH) is a rare developmental disorder of childhood and is characterized by asymmetric enlargement of the epiphyseal cartilage of the long [ncbi.nlm.nih.gov]

Fairbank defined DEH as a developmental disorder which is confined to the medial or lateral half of an epiphysis of a single limb. [jorthoptraumatol.springeropen.com]

Dysplasia epiphysealis hemimelica (DEH) or Trevor's disease is a rare developmental disorder of asymmetric epiphyseal cartilage overgrowth accompanied by an accessory, epiphyseal [ncbi.nlm.nih.gov]

Macrocephaly

We identified a first case of 9q33q34 microduplications in siblings associated with developmental disorders and macrocephaly. [ncbi.nlm.nih.gov]

disorders, 41 children with autism, and a comparison group of 21 children with tuberous sclerosis complex (TSC) or an unspecified seizure disorder were studied. [cambridge.org]

These disorders can be divided into metabolic and developmental categories based on their molecular etiologies. [ncbi.nlm.nih.gov]

Growth Delay-Hydrocephaly-Lung Hypoplasia Syndrome

Orpha Number: 3035 Definition Growth delay - hydrocephaly - lung hypoplasia, also named Game-Friedman- Paradice syndrome, is a rare developmental disorder described in 4 sibs [rareguru.com]

disorder described in 4 sibs so far and characterized by delayed fetal growth, hydrocephaly with patent aqueduct of Sylvius, underdeveloped lungs and various other anomalies [retkebolesti.com]

[…] with the Disease Research Disease at a Glance Symptoms Causes Summary Growth delay - hydrocephaly - lung hypoplasia, also named Game-Friedman-Paradice syndrome, is a rare developmental [rarediseases.info.nih.gov]

Autosomal Recessive Spastic Paraplegia Type 46

Albert Einstein College of Medicine - Pediatric Neurology and Developmental Disorders-Tanjala Gipson and Deepa Menon, Kennedy Krieger Institute and Johns Hopkins University [books.google.com]

Albert Einstein College of Medicine · Pediatric Neurology and Developmental Disorders-Tanjala Gipson and Deepa Menon, Kennedy Krieger Institute and Johns Hopkins University [books.google.com]

Washington University - Dementias-David Knopman, Mayo Clinic - Motorneuron Diseases-Merit Cudkowicz, Massachusetts General Hospital - Paroxysmal Disorders-Solomon Moshe, [books.google.com]

Autosomal Dominant Mental Retardation Type 21

Disorder with Abnormal Behavior, Microcephaly, and Short Stature INTELLECTUAL DEVELOPMENTAL DISORDER WITH CARDIAC ARRHYTHMIA Intellectual Developmental Disorder with Cardiac [rgd.mcw.edu]

Communication Disorders 326 Pervasive Developmental Disorders 331 AttentionDeficit Disorders 337 Disruptive Behavior Disorders 342 Feeding and Eating Disorders of Infancy [books.google.de]

Childhood developmental disorders Developmental disorders of childhood are another large category of mental disorders caused by mutations, deletions, translocations (rearrangements [minddisorders.com]

Williams-Beuren Syndrome

Williams syndrome is a relatively rare neuro-developmental disorder caused by the sporadic deletion of approximately 25-28 genes on chromosome 7. [dur.ac.uk]

In contrast, the neuro-developmental disorder autism is characterised by social withdrawal and lack of interest in socially relevant information. [ncbi.nlm.nih.gov]

Porter, Williams Syndrome, Developmental Disorders and Interventions, 10.1016/B978-0-12-374748-8.00005-6, (163-209), (2010). Marilee A. Martens, Sarah J. [doi.org]

Smith-Magenis Syndrome

This study hypothesized that developmental disorders, such as Smith-Magenis syndrome, may meet criterion for inclusion. [ncbi.nlm.nih.gov]

Smith-Magenis syndrome is a well-known developmental disorder. [ncbi.nlm.nih.gov]

Developmental Reading Disorder

Yule Springer Science & Business Media, ١١‏/١١‏/٢٠١٣ - 286 من الصفحات Perspectives on the Classification of Specific Developmental Disorders is an up-to-date review of the [books.google.com]

It is also known as Developmental Reading Disorder. [dovemed.com]

[…] delay due to hearing loss 315.35 Childhood onset fluency disorder 315.39 Other developmental speech or language disorder 315.4 Developmental coordination disorder 315.5 Mixed [healthprovidersdata.com]

Intellectual Disability

The Working Group further advises that intellectual developmental disorders be incorporated in the larger grouping (parent category) of neurodevelopmental disorders, that [ncbi.nlm.nih.gov]

Munir, The co-occurrence of mental disorders in children and adolescents with intellectual disability/intellectual developmental disorder, Current Opinion in Psychiatry, 29 [doi.org]

Journal of Autism and Developmental Disorders, 32, 283 - 298. [doi.org]

Rett Syndrome

Keywords External Validity Independent Study Developmental Disorder Pervasive Developmental Disorder Rett Syndrome These keywords were added by machine and not by the authors [doi.org]

The author reviews the issue on whether Rett syndrome (RS) is a subtype of pervasive developmental disorders (PDDs). [ncbi.nlm.nih.gov]

Learn More in these related Britannica articles: pervasive developmental disorder >Rett syndrome. [britannica.com]

Axenfeld-Rieger Syndrome Type 3

Disorder Add Citation Views: 1239 Search Journals Articles Advance Search Note: Get EOI for Journal/Conference/ Thesis paper. [citefactor.org]

ARS is an autosomal dominant genetic disease characterized by ocular developmental disorders. [wjgnet.com]

Date: 02 nd August, 2014 Getting Your Journal Indexed Date: 08 th May, 2014 2012 Impact Factor List Date: 28 th April, 2014 Axenfeld Rieger Syndrome: A Rare Developmental [citefactor.org]

Segmental Odontomaxillary Dysplasia

Abstract Segmental odontomaxillary dysplasia (SOD) is a rare, unilateral developmental disorder of the maxilla involving abnormal growth and maturation of the bone, lack of [unboundmedicine.com]

Segmental odontomaxillary dysplasia (SOD) is a rare, unilateral developmental disorder of the maxilla involving abnormal growth and maturation of the bone, lack of one or [ncbi.nlm.nih.gov]

Segmental odontomaxillary dysplasia (SOD) is a rare developmental disorder of the maxilla, and there is little information on its morphological features. [ncbi.nlm.nih.gov]

Organic Delusional Disorder

[…] skills F81.8 Other developmental disorders of scholastic skills F81.9 Developmental disorder of scholastic skills, unspecified F82 Specific developmental disorder of motor [rxpgonline.com]

SYNDROME CONSCIOUSNESS-ALTERING SUBSTANCES PERVASIVE DEVELOPMENTAL DISORDER NOT OTHERWISE SPECIFIED (PDDNOS) PATHOLOGICAL INERTIA Cite this page: N., Pam M.S., "ORGANIC DELUSIONAL [psychologydictionary.org]

Specific disorder of arithmetical skills F81.3 Mixed disorder of scholastic skills F81.8 Other developmental disorders of scholastic skills F81.9 Developmental disorder of [naswma.org]