| 词条 | Acromicric dysplasia |
| 释义 |
| name = Acromicric dysplasia | image = | caption = | synonyms = Acromicric skeletal dysplasia [1] | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} Acromicric dysplasia is an extremely rare inherited disorder characterized by abnormally short hands and feet, growth retardation and delayed bone maturation leading to short stature[2]. Most cases have occurred randomly for no apparent reason (sporadically). However, autosomal dominant inheritance has not been ruled out. According to the disease database, Acromicric dysplasia is synonymous with Geleophysic dysplasia (or Geleophysic Dwarfism) and Focal mucopolysaccharidosis. References1. ^{{cite web |title=Acromicric dysplasia {{!}} Genetic and Rare Diseases Information Center (GARD) – an NCATS Program |url=https://rarediseases.info.nih.gov/diseases/7/index |website=rarediseases.info.nih.gov |accessdate=18 March 2019}} 2. ^{{Cite web|url=https://omim.org/entry/102370|title=OMIM Entry - # 102370 - ACROMICRIC DYSPLASIA; ACMICD|website=omim.org|language=en-us|access-date=2017-07-01}} External links{{Medical resources| DiseasesDB = 32737 | ICD10 = Q77.8 | ICD9 = | ICDO = | OMIM = 102370 | MedlinePlus = | eMedicineSubj = | eMedicineTopic = | GeneReviewsNBK = NBK11168 | GeneReviewsName = Geleophysic Dysplasia | MeshID = C535662 | Orphanet = 969 }}
1 : Rare diseases |
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