Disease #02070 (SHORT (SHORT syndrome (SHORT)), OMIM:269880)

Official abbreviation SHORT
Name SHORT syndrome (SHORT)
OMIM ID 269880
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 6
Associated with 1 gene PIK3R1
Associated tissues -
Disease features -
Remarks -
Date created 2014-09-25 23:29:40 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00046337 - PubMed: Prontera 2015, Journal: Prontera 2015 5-generation family, 1 affected (SHORT syndrome), heterozygous carriers have short stature F yes Italy - - - - - SHORT see paper; SHORT syndrome, high IGFI levels, CNS defects, developmental delay, pronounced progeroid appearance, ... IGF1R C15orf39, EML1, FCRL4, IGF1R, KIR2DL3, KRT5 6 1 B. Augello
00079886 - PubMed: Chudasama 2013 - - - - - - - - - SHORT - PIK3R1 PIK3R1 1 1 Jelena Čalyševa
00079888 - PubMed: Dyment 2013 - F - - - - - - - SHORT - PIK3R1 PIK3R1 1 1 Jelena Čalyševa
00079890 - PubMed: Dyment 2013 - M - - - - - - - SHORT - PIK3R1 PIK3R1 1 1 Jelena Čalyševa
00079891 - PubMed: Bárcena 2014 - M - - - - - - - SHORT - PIK3R1 PIK3R1 1 1 Jelena Čalyševa
00319854 patient PubMed: Goncalves 2022 2-generation family, 1 affected, unaffected heterozygous carrier parents F no Brazil - - - - - SHORT see paper; ..., short stature, ocular depression, Rieger anomaly, teething delay; facial hirsutism, blue sclera, small upslanting palpebral fissures, hypoplastic alae nasi, full cheeks, thin upper lips, large dysplastic ears, micrognathia - PIK3R1 1 1 Juliana Mazzeu
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