Multisystem developmental disorder

Multisystem developmental disorder
Not to be confused with Multiple complex developmental disorder.

Multisystem developmental disorder (MSDD) is a term used by Stanley Greenspan to describe children under age 3 who exhibit signs of impaired communication as in autism, but with strong emotional attachments atypical of autism.[citation needed]

Contents

Other uses of the term

The term multisystem developmental disorder has also been used to describe various developmental disorders, including Cornelia de Lange syndrome,[1] Alagille syndrome,[2] Rubinstein-Taybi syndrome,[3] and Williams syndrome.[4][5]

References

  1. ^ Uzun, H.; Senses, A.; Uluba, M.; Kocabay, K. (Nov 2008). "A newborn with Cornelia de Lange syndrome: a case report" (Free full text). Cases journal 1 (1): 329. doi:10.1186/1757-1626-1-329. PMC 2611981. PMID 19019222. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2611981.  edit
  2. ^ Kamath, B.; Stolle, C.; Bason, L.; Colliton, R.; Piccoli, D.; Spinner, N.; Krantz, I. (Oct 2002). "Craniosynostosis in Alagille syndrome". American journal of medical genetics 112 (2): 176–180. doi:10.1002/ajmg.10608. ISSN 0148-7299. PMID 12244552.  edit
  3. ^ Hendrix, Jd, Jr; Greer, Ke (May 1996). "Rubinstein-Taybi syndrome with multiple flamboyant keloids" (Free full text). Cutis; cutaneous medicine for the practitioner 57 (5): 346–8. ISSN 0011-4162. PMID 8726717. http://www.nlm.nih.gov/medlineplus/headandbrainmalformations.html.  edit
  4. ^ Del, Rio, T; Urbán, Z; Csiszár, K; Boyd, Cd (Aug 1998). "A gene-dosage PCR method for the detection of elastin gene deletions in patients with Williams syndrome". Clinical genetics 54 (2): 129–35. doi:10.1111/j.1399-0004.1998.tb03715.x. ISSN 0009-9163. PMID 9761391.  edit
  5. ^ Scheiber, D.; Fekete, G.; Urban, Z.; Tarjan, I.; Balaton, G.; Kosa, L.; Nagy, K.; Vajo, Z. (Sep 2006). "Echocardiographic findings in patients with Williams-Beuren syndrome". Wiener klinische Wochenschrift 118 (17–18): 538–542. doi:10.1007/s00508-006-0658-2. ISSN 0043-5325. PMID 17009066.  edit

Sources

PubMed

  • Scheeringa, M. (Fall 2001). "The differential diagnosis of impaired reciprocal social interaction in children: a review of disorders". Child psychiatry and human development 32 (1): 71–89. doi:10.1023/A:1017511714145. ISSN 0009-398X. PMID 11579660.  edit

Other sources

v · d · eDevelopmental disorders: Pervasive developmental disorders and autism spectrum (F84, 299)
Main
Diagnoses
Related conditions
Controversies
Diagnostic scales
Lists
Autism-related topics · Fictional characters · People · Speculated historical figures

M: PSO/PSI

mepr

dsrd (o, p, m, p, a, d, s), sysi/epon, spvo

proc(eval/thrp), drug(N5A/5B/5C/6A/6B/6D)



Wikimedia Foundation. 2010.

Игры ⚽ Нужна курсовая?

Look at other dictionaries:

  • Multisystem Developmental Disorder — Multisystem Developmental Disorder, also known as MSDD, is a term coined by Dr. Stanley Greenspan to diagnose children under the age of 3 who exhibit signs of impaired communication as in autism, but with strong emotional attachments atypical of… …   Wikipedia

  • Pervasive developmental disorder — [1] PDD redirects here. For other uses, see PDD (disambiguation). Not to be confused with PDD NOS. Pervasive developmental disorder Classification and external resources ICD 10 F …   Wikipedia

  • Multiple complex developmental disorder — Not to be confused with Multisystem developmental disorder. Multiple complex developmental disorder is a research category, proposed to involve several neurological and psychological symptoms where at least some symptoms are first noticed during… …   Wikipedia

  • List of autism-related topics — This is a list of autism related topics.Conditions and research areas* Asperger syndrome * Autism * Autism Diagnostic Observation Schedule * Autism spectrum * Autism Spectrum Quotient * Causes of autism * Childhood disintegrative disorder *… …   Wikipedia

  • GTF2I — General transcription factor II, i, also known as GTF2I, is a human gene.cite web | title = Entrez Gene: GTF2I general transcription factor II, i| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=2969|… …   Wikipedia

  • GTF2IRD1 — GTF2I repeat domain containing 1, also known as GTF2IRD1, is a human gene.cite web | title = Entrez Gene: GTF2IRD1 GTF2I repeat domain containing 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=9569|… …   Wikipedia

  • LAT2 — Linker for activation of T cells family, member 2, also known as LAT2, is a human gene.cite web | title = Entrez Gene: LAT2 linker for activation of T cells family, member 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene… …   Wikipedia

  • EIF4H — Eukaryotic translation initiation factor 4H, also known as EIF4H, is a human gene.cite web | title = Entrez Gene: EIF4H eukaryotic translation initiation factor 4H| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • CLIP2 — CAP GLY domain containing linker protein 2, also known as CLIP2, is a human gene.cite web | title = Entrez Gene: CLIP2 CAP GLY domain containing linker protein 2| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView… …   Wikipedia

  • MLXIPL — MLX interacting protein like Identifiers Symbols MLXIPL; CHREBP; MIO; MONDOB; WBSCR14; WS bHLH; bHLHd14 External IDs …   Wikipedia

Share the article and excerpts

Direct link
… Do a right-click on the link above
and select “Copy Link”