Results 21 to 30 of about 1,837 (195)
Nasal Reconstruction of a Frontonasal Dysplasia Deformity Using Aesthetic Rhinoplasty Techniques [PDF]
Archives of Plastic Surgery, 2015 Sin Young Song +3 more
doaj +2 more sources
Abstract 7: Novel Stem Cell Model of Frontonasal Dysplasia derived from Pedigree with ALX1-Mutation [PDF]
Plastic and Reconstructive Surgery, Global Open, 2019 Janina Kueper, MD +10 more
doaj +2 more sources
Frontonasal Dysplasia: A Clinical Dilemma. [PDF]
J Maxillofac Oral SurgRao S, Rao S, Bodhey N, Soni N.
europepmc +2 more sources
The Egyptian Journal of Radiology and Nuclear Medicine, 2021 Background Encephaloceles are herniation of brain parenchyma through the defect in the dura and the skull bones. This case report reveals a rare association of frontonasal encephalocele, subependymal nodular heterotopias and cerebellar dysplasia with ...
Kunwar Pal Singh +2 more
doaj +1 more source
Orbital box osteotomy in frontonasal dysplasia with severe hypertelorism: Our first experience
Journal of Cleft Lip Palate and Craniofacial Anomalies, 2023 Frontonasal dysplasia (FND) is a rare craniofacial deformity, including severe hypertelorism. We herein presented the case of a 6-year-old female patient with FND and Grade III hypertelorism who underwent a four-wall-orbital box osteotomy with a ...
I Made Suka Adnyana +2 more
doaj +1 more source
Molecular Ecology, Volume 32, Issue 21, Page 5798-5811, November 2023., 2023 Abstract Evolutionary novelties—derived traits without clear homology found in the ancestors of a lineage—may promote ecological specialization and facilitate adaptive radiations. Examples for such novelties include the wings of bats, pharyngeal jaws of cichlids and flowers of angiosperms.
Ralf F. Schneider +4 more
wiley +1 more source
A developmental and genetic classification for malformations of cortical development: update 2012. [PDF]
, 2012 Malformations of cerebral cortical development include a wide range of developmental disorders that are common causes of neurodevelopmental delay and epilepsy. In addition, study of these disorders contributes greatly to the understanding of normal brain
Barkovich, A James +4 more
core +3 more sources
Craniofrontonasal dysplasia: A case report
Pediatric Discovery, Volume 1, Issue 1, June 2023., 2023 Abstract Craniofrontonasal dysplasia (CFND) is a rare congenital malformation, which has a wide array of symptoms that can vary drastically between patients. These include coronal synostosis with associated brachycephaly, hypertelorism, cleft lip and palate, and limb malformations, among others.
Kanad Ghosh +4 more
wiley +1 more source
Regulating Retinoic Acid Availability during Development and Regeneration: The Role of the CYP26 Enzymes. [PDF]
, 2020 This review focuses on the role of the Cytochrome p450 subfamily 26 (CYP26) retinoic acid (RA) degrading enzymes during development and regeneration. Cyp26 enzymes, along with retinoic acid synthesising enzymes, are absolutely required for RA homeostasis
Roberts, C
core +4 more sources
Frontiers in Genetics, 2023 Craniofrontonasal Syndrome is a very rare dominant X-linked genetic disorder characterized by symptoms such as hypertelorism, craniosynostosis, eye alterations, bifid nose tip, and longitudinal ridging and splitting of nails.
Harry Pachajoa +4 more
doaj +1 more source