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Craniofacial Dysostosis - Complications
Research News and Information
Definition of 'Craniofacial Dysostosis'An autosomal dominant disorder characterized by acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, and hypoplastic maxilla with relative mandibular prognathism. (Dorland, 27th ed) Common names: Craniofacial Dysostosis; Crouzon's Disease; Crouzons Disease; Disease, Crouzon's; Crouzon Disease; Disease, Crouzon; Dysostosis, Craniofacial; Craniofacial Dysostoses; Dysostoses, Craniofacial |
Sunday, November 22, 2009
29 Jun 2009
We report on a 6-month-old boy with craniosynostosis, pseudohypoparathyroidism type 1a (PHP1A), and a GNAS gene mutation. He had synostoses of the coronal, frontal, and sagittal sutures, brachyturricephaly, and hydrocephaly. He also had congenital ... Read more...
Comparison of periodontal parameters in individuals with syndromic craniosynostosis.
30 Dec 2008
Craniosynostosis syndromes are characterized by premature closure of one or more cranial sutures, associated with other malformations, the most frequent of which are the Crouzon and Apert syndromes. Few studies in the literature have addressed the ... Read more...
[Experience of midfacial distraction osteogenesis in upper airway stenosis]
13 Apr 2008
OBJECTIVE: To investigate the therapeutic effects of upper airway stenosis after Le Fort III osteotomy and midfacial distraction osteogenesis (DO). METHODS: Eleven cases (age, 5-16 yrs) with severe midface dysostosis complicated with exophthalmos, ... Read more...
Latest indexed articles for 'Craniofacial Dysostosis - Complications'
These are the very latest articles for this heading:
- Combined internal and external distraction of the midface for the treatment of Crouzon syndrome and critical obstructive sleep apnea: a case report.
30 Aug 2009 - Boy with pseudohypoparathyroidism type 1a caused by GNAS gene mutation (deltaN377), Crouzon-like craniosynostosis, and severe trauma-induced bleeding.
29 Jun 2009 - Comparison of periodontal parameters in individuals with syndromic craniosynostosis.
30 Dec 2008 - Tracheal intubation in a patent with Crouzon's syndrome using LMA-Fastrach with the Cook Airway Exchange Catheter.
30 Dec 2008 - Unusual cause of near cardiac arrest following craniofacial reconstruction.
29 Nov 2008 - [Experience of midfacial distraction osteogenesis in upper airway stenosis]
13 Apr 2008 - Monoblock craniofacial internal distraction in a child with Pfeiffer syndrome: a case report.
30 Mar 2008 - Care of a parturient with preeclampsia, morbid obesity, and Crouzon's syndrome.
2 Mar 2008 - Physical and oral characteristics of Crouzon syndrome, Apert syndrome, and Pierre Robin sequence.
28 Feb 2008 - Midface osteotomy versus distraction: the effect on speech, nasality, and velopharyngeal function in craniofacial dysostosis.
19 Jan 2008 - Papilledema in patients with Apert, Crouzon, and Pfeiffer syndrome: prevalence, efficacy of treatment, and risk factors.
30 Dec 2007 - Detection of important venous collaterals by computed tomography venogram in multisutural synostosis. Case report and review of the literature.
29 Nov 2007 - Crouzon with acanthosis nigricans. Further delineation of the syndrome.
30 Oct 2007 - Brain malformation in syndromic craniosynostoses, a primary disorder of white matter: a review.
18 Sep 2007 - A novel model surgery technique for LeFort III advancement.
30 Aug 2007 - Visual manifestations of craniofrontonasal dysplasia.
29 Jun 2007 - [Crouzon syndrome: factors related to the neuropsychological development and to the quality of life]
30 May 2007 - Morphology and growth of the mandible in Crouzon, Apert, and Pfeiffer syndromes.
30 Dec 2006 - Sinus pericranii associated with craniosynostosis.
30 Dec 2006 - Severe dehydration and acute renal failure associated with external ventricular drainage of cerebrospinal fluid in children.
29 Sep 2006
See a longer list of these articles.
Technical information about 'Craniofacial Dysostosis'
Definition: An autosomal dominant disorder characterized by acrocephaly, exophthalmos, hypertelorism, strabismus, parrot-beaked nose, and hypoplastic maxilla with relative mandibular prognathism. (Dorland, 27th ed)
Descriptor UI: D003394
Alternative terms: Craniofacial Dysostosis; Crouzon's Disease; Crouzons Disease; Disease, Crouzon's; Crouzon Disease; Disease, Crouzon; Dysostosis, Craniofacial; Craniofacial Dysostoses; Dysostoses, Craniofacial;
Allowable Qualifiers: blood; cerebrospinal fluid; chemically induced; classification; complications; diagnosis; diet therapy; drug therapy; economics; embryology; enzymology; ethnology; etiology; genetics; history; immunology; metabolism; microbiology; mortality; nursing; epidemiology; parasitology; pathology; physiopathology; prevention & control; psychology; radiography; radionuclide imaging; radiotherapy; rehabilitation; surgery; therapy; ultrastructure; urine; veterinary; ultrasonography; virology;
Tree Number: C05.116.099.370.231; C05.660.207.231; C16.131.621.207.231;
Technical Notes: do not use /congen & do not coord with INFANT, NEWBORN, DISEASES; "craniofacial dysmorphism" does not go here: index under FACIAL BONES /abnorm + SKULL /abnorm but not also under ABNORMALITIES, MULTIPLE