Crouzonodermoskeletal syndrome - Wikipedia
Crouzonodermoskeletal syndrome is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans.
克鲁宗综合征 - 百度百科
克鲁宗综合征 (Crouzon Syndrome)是一组由多发性颅部骨缝和面部骨缝早闭引起的颅部和面部复合畸形的症候群，常伴颅内压增高症。 1921年Crouzon首先报道了此病，故称Crouzon综合征，又称鹦鹉头综合征、Virchow综合征、先天性尖头并指 (趾)畸形综合征、狭颅综合征等，是以颅骨缝闭合过早、上颌发育不良以及眼球突出等为主要特征的一种综合征。 畸形主要表现为上颌骨严重后缩、突眼和反牙合。
Crouzon syndrome with acanthosis nigricans - MedlinePlus
Crouzon syndrome with acanthosis nigricans is a disorder characterized by the premature joining of certain bones of the skull (craniosynostosis) during development and a skin condition called acanthosis nigricans. Explore symptoms, inheritance, genetics of this condition.
Crouzon Syndrome - StatPearls - NCBI Bookshelf
2023年8月7日 · Crouzon syndrome is a genetically inherited syndrome characterized by craniosynostosis (premature fusion of coronal sutures) resulting in the skull and facial deformities. The syndrome was first described in 1912 by French physician Octave Crouzon when he identified both a mother and daughter with what was originally called “craniofacial ...
Crouzon Syndrome: Symptoms, Causes & Outlook - Cleveland Clinic
2021年12月10日 · Crouzon syndrome is a rare genetic disorder that causes the fibrous joints (sutures) between your baby’s skull bones to fuse too early (craniosynostosis). When your baby’s sutures fuse too early, it prevents their skull from growing properly. This can affect the shape of their head and face.
Crouzon syndrome - DermNet
2015年5月6日 · Skeletal abnormalities, including the fusion of the spinal column. The main dermatological sign of Crouzon syndrome is acanthosis nigricans, in which there is thickened, hyperpigmented skin with a velvety feel affecting the neck, torso, and face. It usually occurs by the onset of puberty. How is Crouzon syndrome diagnosed?
Crouzon syndrome with acanthosis nigricans: a case report and ...
Crouzon syndrome with acanthosis nigricans is an autosomal dominant disease, with typical features of classic Crouzon craniosynostosis, verrucous hyperplasia, and hyperpigmentation of the skin. While several mutations in FGFR2 cause classic Crouzon ...
Crouzono-dermo-skeletal syndrome, Crouzon syndrome with …
2020年6月3日 · The molecular and genetic basis of fibroblast growth factor receptor 3 disorders: the achondroplasia family of skeletal dysplasias, Muenke craniosynostosis, and Crouzon syndrome with acanthosis nigricans.
Crouzon syndrome with acanthosis nigricans: a case-based …
Background: Crouzon syndrome with acanthosis nigricans also named Crouzono-dermo-skeletal is a clinically and genetically distinct entity. It associates a craniofacial phenotype to anomalies of the skin and long bones. This syndrome is due to a specific mutation in FGFR3 gene that can be identified by genetic testing.
Crouzon Syndrome (CS) with Acanthosis Nigricans is a disorder characterised by the premature joining of certain bones of the skull {Craniosynostosis (CSO)} during development and a skin condition called Acanthosis Nigricans. Two cases of CSO with abnormal facies were referred to the present tertiary genetic centre.
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