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Apert's syndrome, 03/2004
Apert's syndrome (acrocephalosyndactyly) is a rare congenital disorder characterized by craniosynostosis, mid-facial malformations and symmetrical syndactyly.... 
Apert’s Syndrome, Cerebral cortical atrophy, Bone changes. dv04031 | Dermatology
Journal
Journal of Cranio-Maxillo-Facial Surgery, ISSN 1010-5182, 10/2016, Volume 44, Issue 10, pp. 1567 - 1575
Journal Article
Human Mutation, ISSN 1059-7794, 1999, Volume 14, Issue 2, pp. 115 - 125
Journal Article
JOURNAL OF CRANIOFACIAL SURGERY, ISSN 1049-2275, 03/2019, Volume 30, Issue 2, pp. 508 - 509
Apert syndrome is one of the acrocephalosyndactilia syndromes that is characterized with calvarial an extremity deformities. Anesthesia management of this... 
SURGERY | Apert syndrome | hyponatremia | craniosynostosis surgery
Journal Article
Child's Nervous System, ISSN 0256-7040, 2019, Volume 35, Issue 3, pp. 565 - 567
BackgroundApert syndrome is a rare form of syndromic craniosynostosis, also known as acrocephalosyndactyly, which is a disorder characterized by a unique set... 
Apert syndrome | Fibroblast growth factor receptors (FGFR)2 | Atypical case | Craniosynostosis | SURGERY | DOMAIN | GROWTH-FACTOR RECEPTOR-3 | PEDIATRICS | MUTATIONS | CLINICAL NEUROLOGY | Craniosynostoses | Usage | Analysis | Acrocephalosyndactylia | Physiological aspects | Fibroblast growth factors | Genetic aspects | Diagnosis | Multiple abnormalities | Genetic screening
Journal Article
Journal of the European Academy of Dermatology and Venereology, ISSN 0926-9959, 06/2011, Volume 25, Issue 6, pp. 637 - 646
Acne, one of the most common skin disorders, is also a cardinal component of many systemic diseases or syndromes. Their association illustrates the nature of... 
PAPA syndrome | Apert syndrome | acne | insulin resistance | PCO syndrome | SAPHO syndrome | POLYCYSTIC-OVARY-SYNDROME | OSTEITIS SAPHO SYNDROME | CONGENITAL ADRENAL-HYPERPLASIA | HAIR-AN SYNDROME | SEBACEOUS GLAND | DERMATOLOGY | PYOGENIC ARTHRITIS | PYODERMA-GANGRENOSUM | ANDROGEN EXCESS DISORDERS | 13-CIS RETINOIC ACID | Pyoderma Gangrenosum - drug therapy | Adrenal Hyperplasia, Congenital - drug therapy | Arthritis, Infectious - drug therapy | Acne Vulgaris - etiology | Alopecia - complications | Humans | Acanthosis Nigricans - complications | Acrocephalosyndactylia - genetics | Hyperandrogenism - drug therapy | Acne Vulgaris - complications | Polycystic Ovary Syndrome - complications | Polycystic Ovary Syndrome - drug therapy | Hyperandrogenism - surgery | Female | Dermatitis, Seborrheic - complications | Acanthosis Nigricans - drug therapy | Acquired Hyperostosis Syndrome - complications | Insulin Resistance | Acne Vulgaris - drug therapy | Adrenal Hyperplasia, Congenital - complications | Acrocephalosyndactylia - complications | Syndrome | Hirsutism - complications | Acanthosis Nigricans - surgery | Arthritis, Infectious - complications | Hyperandrogenism - complications | Pyoderma Gangrenosum - complications | Medical colleges | Insulin resistance | Fibroblast growth factors | Genetic disorders | Stein-Leventhal syndrome | Acne
Journal Article
Journal of Medical and Scientific Research, ISSN 2321-1326, 04/2015, Volume 3, Issue 2, pp. 70 - 74
Craniosynostosis is due to premature closure of the cranial sutures. The radiological findings of a 3-year-old girl with a small head, triangular frontal... 
craniosynostosis | syndactyly | Apert syndrome
Journal Article
Pakistan Paediatric Journal, ISSN 0304-4904, 03/2015, Volume 39, Issue 1, pp. 53 - 56
Journal Article
Journal of Krishna Institute of Medical Sciences University, ISSN 2231-4261, 01/2019, Volume 8, Issue 1, pp. 95 - 99
Apert syndrome is a congenital acrocephalosyndactyly syndrome. It is mainly presented by craniosynostosis, syndactyly of the hands and feet and dysmorphic... 
Acrocephalosyndactyly | Craniosynostosis | Apert Syndrome | Omphalocele
Journal Article
Child's Nervous System, ISSN 0256-7040, 6/2018, Volume 34, Issue 6, pp. 1247 - 1250
Apert syndrome is one of the most common craniosynostosis syndrome caused by mutation in genes encoding fibroblast growth factor receptor 2 (FGFR2).... 
Neurosciences | Apert syndrome | Medicine & Public Health | Neurosurgery | RASopathies | RAS/MAPK signaling pathway | Sturge-Weber syndrome | Fibronectin | Case studies | Cellular signal transduction | Diagnosis | Research
Journal Article
Pediatriya, ISSN 0479-7876, 2014, Volume 54, Issue 4, pp. 36 - 38
Journal Article
Journal Article
Ultrasound in Obstetrics & Gynecology, ISSN 0960-7692, 09/2017, Volume 50, Issue S1, pp. 312 - 312
Journal Article
Journal of Oral Biology and Craniofacial Research, ISSN 2212-4268, 2018, Volume 8, Issue 3, pp. 194 - 199
Abstract Apert syndrome is one of the several genetic syndromes associated with craniosynostosis, a condition that includes premature fusion of one or multiple... 
Otolaryngology | Genetic disorder | Apert syndrome | Craniosynostosis | FGFR2 | Acrocephalosyndactylia | Genetic aspects | Diagnosis | Research | Gene mutations
Journal Article
Journal of Craniofacial Surgery, ISSN 1049-2275, 07/2016, Volume 27, Issue 5, pp. 1125 - 1134
Journal Article
International Journal of Oral & Maxillofacial Surgery, ISSN 0901-5027, 03/2019, Volume 48, Issue 3, pp. 309 - 321
The facial malformations of Crouzon syndrome involve the entire cranio-orbito-zygomatic region. The detailed sequence of changes in orbit, zygoma, and maxilla... 
midface | zygoma | orbit | maxilla | Crouzon syndrome | SURGERY | APERT | DYSMORPHOLOGY | CRANIAL BASE | ADVANCEMENT | DISTRACTION OSTEOGENESIS | OSTEOTOMY | DENTISTRY, ORAL SURGERY & MEDICINE | FACIAL GROWTH | EXPANSION | Medical colleges | Surgery, Plastic | Analysis
Journal Article