Literature DB >> 9527308

A cephalometric evaluation of craniofacial morphology in familial dysautonomia.

E Mass1, I Brin, L Belostoky, C Maayan, N Gadoth.   

Abstract

OBJECTIVE: The purpose of this study was to delineate the craniofacial and dentoalveolar morphology of patients with familial dysautonomia (FD) in order to contribute to the understanding of the association between progressive sensory and autonomic neuropathy and the characteristic appearance of the dysautonomic face. PATIENTS: The study group comprised 32 patients with FD (15 females and 17 males; mean age 10.8 years, SD 3.5 years, range 5.8-19.8 years).
DESIGN: Lateral cephalograms from each patient were traced twice. The means of the two measurements were compared with homologous cephalometric normal values of ethnic-specific and classical norms from the literature.
RESULTS: In some parameters, the craniofacial morphology of the FD group was significantly different from the classical norms. There was a pronounced retrognathism in the mandible and a steep mandibular plane angle. The skeletal features of FD patients more closely resembled those of their ethnic group, although they were more retrognathic, and the mandibular growth axis was more horizontal. The incisors of these patients were more retropositioned and retroclined than were those of their healthy counterparts.
CONCLUSIONS: The results suggest an insufficiency of the expected dentoalveolar compensatory mechanism that usually helps to bridge skeletal discrepancies. It is postulated that the neuropathy is probably the important factor in the lack of this compensatory mechanism.

Entities:  

Mesh:

Year:  1998        PMID: 9527308     DOI: 10.1597/1545-1569_1998_035_0120_aceocm_2.3.co_2

Source DB:  PubMed          Journal:  Cleft Palate Craniofac J        ISSN: 1055-6656


  7 in total

1.  Familial dysautonomia model reveals Ikbkap deletion causes apoptosis of Pax3+ progenitors and peripheral neurons.

Authors:  Lynn George; Marta Chaverra; Lindsey Wolfe; Julian Thorne; Mattheson Close-Davis; Amy Eibs; Vickie Riojas; Andrea Grindeland; Miranda Orr; George A Carlson; Frances Lefcort
Journal:  Proc Natl Acad Sci U S A       Date:  2013-10-30       Impact factor: 11.205

Review 2.  Respiratory care in familial dysautonomia: Systematic review and expert consensus recommendations.

Authors:  Mikhail Kazachkov; Jose-Alberto Palma; Lucy Norcliffe-Kaufmann; Bat-El Bar-Aluma; Christy L Spalink; Erin P Barnes; Nancy E Amoroso; Stamatela M Balou; Shay Bess; Arun Chopra; Rany Condos; Ori Efrati; Kathryn Fitzgerald; David Fridman; Ronald M Goldenberg; Ayelet Goldhaber; David A Kaufman; Sanjeev V Kothare; Jeremiah Levine; Joseph Levy; Anthony S Lubinsky; Channa Maayan; Libia C Moy; Pedro J Rivera; Alcibiades J Rodriguez; Gil Sokol; Mark F Sloane; Tina Tan; Horacio Kaufmann
Journal:  Respir Med       Date:  2018-06-21       Impact factor: 3.415

3.  ELP1 Splicing Correction Reverses Proprioceptive Sensory Loss in Familial Dysautonomia.

Authors:  Elisabetta Morini; Dadi Gao; Connor M Montgomery; Monica Salani; Chiara Mazzasette; Tobias A Krussig; Brooke Swain; Paula Dietrich; Jana Narasimhan; Vijayalakshmi Gabbeta; Amal Dakka; Jean Hedrick; Xin Zhao; Marla Weetall; Nikolai A Naryshkin; Gregory G Wojtkiewicz; Chien-Ping Ko; Michael E Talkowski; Ioannis Dragatsis; Susan A Slaugenhaupt
Journal:  Am J Hum Genet       Date:  2019-03-21       Impact factor: 11.025

4.  Obstructive Sleep-Disordered Breathing Is More Common than Central in Mild Familial Dysautonomia.

Authors:  Max J Hilz; Sebastian Moeller; Susanne Buechner; Hanna Czarkowska; Indu Ayappa; Felicia B Axelrod; David M Rapoport
Journal:  J Clin Sleep Med       Date:  2016-12-15       Impact factor: 4.062

5.  A neuron autonomous role for the familial dysautonomia gene ELP1 in sympathetic and sensory target tissue innervation.

Authors:  Marisa Z Jackson; Katherine A Gruner; Charles Qin; Warren G Tourtellotte
Journal:  Development       Date:  2014-06       Impact factor: 6.868

Review 6.  Oral manifestations, dental management, and a rare homozygous mutation of the PRDM12 gene in a boy with hereditary sensory and autonomic neuropathy type VIII: a case report and review of the literature.

Authors:  Karim Elhennawy; Seif Reda; Christian Finke; Luitgard Graul-Neumann; Paul-Georg Jost-Brinkmann; Theodosia Bartzela
Journal:  J Med Case Rep       Date:  2017-08-15

7.  Familial Dysautonomia: Mechanisms and Models.

Authors:  Paula Dietrich; Ioannis Dragatsis
Journal:  Genet Mol Biol       Date:  2016-08-04       Impact factor: 1.771

  7 in total

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