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abnormal development (of organs or cells) or an abnormal structure resulting from such growth

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/04/22 20:08:49」(JST)

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1. 先天性股関節脱臼：治療および転帰 developmental dysplasia of the hip treatment and outcome
2. 線維筋異形成症の臨床症状および診断 clinical manifestations and diagnosis of fibromuscular dysplasia
3. 腎動脈の線維筋異形成症の治療 treatment of fibromuscular dysplasia of the renal arteries
4. Barrett's esophagus: Surveillance and management
5. 気管支肺異形成症の予防 prevention of bronchopulmonary dysplasia

Characterization of an acromesomelic dysplasia, Grebe type case: novel mutation affecting the recognition motif at the processing site of GDF5.

Martinez-Garcia M1, Garcia-Canto E, Fenollar-Cortes M, Aytes AP, Trujillo-Tiebas MJ.
Journal of bone and mineral metabolism.J Bone Miner Metab.2015 Aug 15. [Epub ahead of print]
Acromesomelic dysplasia, Grebe type is a very rare skeletal dysplasia characterized by severe dwarfism with marked micromelia and deformation of the upper and lower limbs, with a proximodistal gradient of severity. CDMP1 gene mutations have been associated with Grebe syndrome, Hunter-Thompson syndro
PMID 26275437

Homozygous sequence variants in the NPR2 gene underlying Acromesomelic dysplasia Maroteaux type (AMDM) in consanguineous families.

Irfanullah1, Umair M1, Khan S2, Ahmad W1.
Annals of human genetics.Ann Hum Genet.2015 Jul;79(4):238-44. doi: 10.1111/ahg.12116. Epub 2015 May 11.
Acromesomelic dysplasia Maroteaux type (AMDM) is an autosomal recessive skeletal disorder characterized by disproportionate short stature with shortening of the acromesomelic sections of the limbs. AMDM is caused by mutations in the NPR2 gene located on chromosome 9p21-p12. The gene encodes the natr
PMID 25959430

Stange K1,2, Désir J3, Kakar N4, Mueller TD5, Budde BS6, Gordon CT7,8, Horn D9, Seemann P1,2, Borck G10.
Orphanet journal of rare diseases.Orphanet J Rare Dis.2015 Jun 24;10:84. doi: 10.1186/s13023-015-0299-5.
BACKGROUND: Grebe dysplasia, Hunter-Thompson dysplasia, and du Pan dysplasia constitute a spectrum of skeletal dysplasias inherited as an autosomal recessive trait characterized by short stature, severe acromesomelic shortening of the limbs, and normal axial skeleton. The majority of patients with t
PMID 26105076

Management of general anesthesia for a patient with Maroteaux type acromesomelic dysplasia complicated with obstructive sleep apnea syndrome and hereditary myopathy

Translational research of C-type natriuretic peptide (CNP) into skeletal dysplasias

Mutations in the transmembrane natriuretic peptide receptor NPR-B impair skeletal growth and cause acromesomelic dysplasia, type Maroteaux