Category:Apert syndrome
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congenital disorder of digestive system | |||||
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Subcategories
This category has only the following subcategory.
S
- Syndactyly in Apert syndrome (27 F)
Media in category "Apert syndrome"
The following 59 files are in this category, out of 59 total.
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1 Encontro de Aperts no Brasil - março de 2018.jpg 845 × 404; 375 KB
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Acrocéphalosyndactylie 10.jpg 921 × 764; 263 KB
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Acrocéphalosyndactylie 2.jpg 860 × 904; 258 KB
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Acrocéphalosyndactylie 3.jpg 688 × 650; 125 KB
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Acrocéphalosyndactylie 4.jpg 500 × 553; 76 KB
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Acrocéphalosyndactylie 5.jpg 780 × 705; 183 KB
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Acrocéphalosyndactylie 7.jpg 979 × 977; 274 KB
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Acrocéphalosyndactylie 8.jpg 643 × 1,002; 170 KB
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Acrocéphalosyndactylie 9.jpg 538 × 969; 150 KB
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Alantar Acrocephalosyndactylie 1.jpg 859 × 1,220; 112 KB
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Alantar Acrocephalosyndactylie 2.jpg 675 × 1,102; 129 KB
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Apert Ruh 1.jpg 1,219 × 1,604; 529 KB
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Apert Ruh 2.jpg 1,623 × 2,348; 778 KB
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Apert Syndrome 1.jpg 574 × 864; 167 KB
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Apert Syndrome 2.jpg 589 × 874; 178 KB
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Apert Syndrome 3.jpg 577 × 779; 154 KB
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Apert Syndrome 4.jpg 923 × 773; 299 KB
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Apert Syndrome 5.jpg 926 × 784; 284 KB
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Casazza 1.jpg 943 × 1,308; 306 KB
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Casazza 2.jpg 1,017 × 1,517; 288 KB
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Casazza 3.jpg 1,048 × 1,511; 333 KB
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Casazza 4.jpg 920 × 1,319; 277 KB
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Casazza 6.jpg 1,016 × 1,007; 152 KB
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Craniofacial-divergence-by-distinct-prenatal-growth-patterns-in-Fgfr2-mutant-mice-1471-213X-14-8-S3.ogv 0.0 s, 848 × 480; 13.79 MB
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Craniofacial-divergence-by-distinct-prenatal-growth-patterns-in-Fgfr2-mutant-mice-1471-213X-14-8-S4.ogv 0.0 s, 848 × 480; 15.98 MB
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Craniofacial-divergence-by-distinct-prenatal-growth-patterns-in-Fgfr2-mutant-mice-1471-213X-14-8-S5.ogv 0.0 s, 848 × 480; 15.24 MB
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Craniofacial-divergence-by-distinct-prenatal-growth-patterns-in-Fgfr2-mutant-mice-1471-213X-14-8-S6.ogv 0.0 s, 848 × 480; 16.29 MB
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Craniofacial-divergence-by-distinct-prenatal-growth-patterns-in-Fgfr2-mutant-mice-1471-213X-14-8-S8.ogv 0.0 s, 848 × 480; 14.78 MB
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Craniofacial-divergence-by-distinct-prenatal-growth-patterns-in-Fgfr2-mutant-mice-1471-213X-14-8-S9.ogv 0.0 s, 848 × 480; 14.9 MB
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Fini 1.jpg 766 × 1,073; 289 KB
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Fini 4.jpg 723 × 771; 130 KB
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Gadelius 1.jpg 1,220 × 870; 649 KB
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Gadelius 12.jpg 1,223 × 1,658; 972 KB
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Gadelius 14.jpg 1,219 × 1,956; 1.11 MB
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Gadelius 16.jpg 573 × 785; 240 KB
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Gadelius 17.jpg 563 × 776; 235 KB
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Gadelius 18.jpg 582 × 1,073; 362 KB
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Gadelius 19.jpg 577 × 1,067; 350 KB
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Gadelius 2.jpg 580 × 904; 325 KB
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Gadelius 20.jpg 841 × 1,400; 874 KB
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Gadelius 21.jpg 611 × 616; 286 KB
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Gadelius 22.jpg 733 × 1,027; 497 KB
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Gadelius 3.jpg 581 × 915; 317 KB
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Gadelius 7.jpg 1,213 × 1,847; 721 KB
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Gadelius 9.jpg 1,208 × 769; 428 KB
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Liceaga 1.jpg 502 × 1,302; 130 KB
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Liceaga 2.jpg 771 × 978; 184 KB
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Park Powers 1.jpg 907 × 1,390; 306 KB
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Park Powers 2.jpg 1,280 × 1,477; 379 KB
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Park Powers 3.jpg 1,280 × 1,647; 286 KB
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Park Powers 6.jpg 1,207 × 893; 196 KB
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Patient with Apert syndrome.jpg 800 × 600; 93 KB
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PMC4640438 1657-9534-cm-46-03-00150-gf04.png 328 × 376; 207 KB
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Précis de psychiatrie 3.jpg 683 × 934; 152 KB
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Précis de psychiatrie 4.jpg 777 × 899; 162 KB
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Salterain 1.jpg 1,156 × 1,661; 213 KB
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Salterain 2.jpg 1,135 × 1,681; 220 KB
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Syphilis and Marriage 10 (Malformation).jpg 1,420 × 2,182; 1.03 MB
Categories:
- Cell surface receptor deficiencies
- Acrocephalosyndactyly
- Congenital diseases and disorders of eye, ear, face and neck
- Hypertelorism
- Diseases and disorders of the human teeth
- Diseases and disorders of the ears, nose and throat
- Hearing loss with craniofacial syndromes
- Kleeblattschaedel
- Brachycephaly
- Scaphocephaly