[HTML][HTML] Craniofacial disorders and dysplasias: Molecular, clinical, and management perspectives

SO Akintoye, AO Adisa, CU Okwuosa, M Mupparapu - Bone Reports, 2024 - Elsevier
There is a wide spectrum of craniofacial bone disorders and dysplasias because
embryological development of the craniofacial region is complex. Classification of …

Marfan Syndrome with Aortic Root Disease, Severe Heart Failure and Aortic Dissection-Two Case Reports

PO Njoku, NC Mbadiwe, BJ Onwubere… - Nigerian Journal of …, 2022 - journals.lww.com
Marfan syndrome is an uncommon inheritable connective tissue disease which affects the
cardiovascular system. This paper presents two cases of Marfan Syndrome with …

Shape of the dilated aorta in children with bicuspid aortic valve

CR Mart, BE McNerny - Annals of pediatric cardiology, 2013 - journals.lww.com
Background: The dilated aorta in adults with bicuspid aortic valve has been shown to have
different shapes, but it is not known if this occurs in children. This observational study was …

[HTML][HTML] Ghent criteria an aid to diagnose latent systemic diseases in Marfan syndrome

G Ramlingam… - Journal of Clinical and …, 2015 - ncbi.nlm.nih.gov
General examination revealed height measurement of 174.5 cms (upper segment-72.5 cms
and lower segment-102 cm, long and slender extremities [Table/Fig-1] with spider-like …

Dental findings in marfan syndrome: a case report

B Bostancı, N Ünlü, E Korkut - Journal of Istanbul University Faculty …, 2017 - dergipark.org.tr
Marfan syndrome is an autosomal dominant disorder of connective tissue primarily
characterized with anomalies affecting the musculoskeletal system, the cardiovascular …

Craniofacial disorders and dysplasias: Molecular, clinical, and management perspectives

M Mupparapu - Bone Reports, 2024 - repository.upenn.edu
There is a wide spectrum of craniofacial bone disorders and dysplasias because
embryological development of the craniofacial region is complex. Classification of …

Full-mouth rehabilitation with implant-prosthesis in marfan syndrome patient: clinical report and literature review

A Kutkut, R Abu-Eid, L Sharab… - Journal of Oral …, 2020 - meridian.allenpress.com
The purpose of this case report is to present implant-retained maxillary and mandibular
complete overdentures in a patient with Marfan syndrome. The patient initially presented …

[HTML][HTML] Management of unilateral temporomandibular joint ankylosis & orthomorphic correction in a patient with Marfan syndrome: A rare case report

BM Rudagi, J Rishabh, M Arif, C Namrata… - International Journal of …, 2020 - Elsevier
Introduction Marfan syndrome (MFS) is a disorder of the connective tissue that is inherited in
an autosomal dominant fashion and is caused by mutations in the gene coding for fibrillin-1 …

A novel fibrillin-1 gene mutation leading to Marfan syndrome in a Korean girl

HK Nam, MH Nam, KS Ha, YJ Rhie… - Annals of Clinical & …, 2017 - Assoc Clin Scientists
Marfan syndrome is an autosomal dominant genetic disorder caused by a connective tissue
defect. A nine-year-old girl was referred to our pediatric endocrinology clinic for tall stature …

[PDF][PDF] Marfan Syndrome: A Case Report.

MG Ortaköylü, T Özen, BA Bağcı… - Respiratory Case …, 2020 - jag.journalagent.com
Marfan syndrome (MFS) is a connective tissue disorder inherited by autosomal dominant
pattern that affects primarily cardiovascular, ocular, musculoskeletal and nervous systems …