Disease #05314 (Turner (Turner syndrome))

Official abbreviation Turner
Name Turner syndrome
OMIM ID -
Inheritance Somatic mosaicism
Individuals reported having this disease 7
Phenotype entries for this disease 4
Associated with 0 genes -
Associated tissues -
Disease features -
Remarks -
Date created 2017-08-07 17:16:21 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

7 entries on 1 page. Showing entries 1 - 7.
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00115222 - SHOX Lab Heidelberg, unpublished - - - United States - - - - - Turner Turner syndrom (TS) SHOX SHOX 1 7 Ralph Roeth
00115270 - pers. comm. - - - - - - - - - Turner - SHOX SHOX 1 1 Ralph Roeth
00115271 - pers. comm. - - - - - - - - - Turner - SHOX SHOX 1 1 Ralph Roeth
00115272 - pers. comm. - - - - - - - - - Turner Turner syndrom (TS) SHOX SHOX 1 1 Ralph Roeth
00115276 - pers. comm. - - - - - - - - - Turner Turner syndrom (TS) SHOX SHOX 1 3 Ralph Roeth
00288831 patient PubMed: Kaczorowska 2016 - F - Poland - - - - - DMD, Turner classical 45,X Turner syndrome, short neck, low posterior hairline, wide position of nipples, aortic coarctation, feet lymphedema, infantile-onset motor developmental delay, intellectual disability,d early calf muscular hypertrophy DMD DMD 1 1 Johan den Dunnen
00427143 patient PubMed: Lamanna 2022 - rF - Italy India - - - - DMD, Turner see paper; birth at term, diagnosed prenatally ambiguous genitalia; Turner syndrome, no typical dysmorphic TS features (except genitourinary system; 3y-increasing difficulty walking, running, jumping and climbing stairs, proximal upper/lower extremity muscle weakness, positive Gowers’ sign; 30x raised serum creatine kinase DMD DMD 1 1 Johan den Dunnen
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