Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature | Italian Journal of Pediatrics | Full Text
Ellas opinan: SuperAina y el síndrome de Loeys-Dietz
Arthrogryposis as neonatal presentation of Loeys-Dietz syndrome due to a novel TGFBR2 mutation - ScienceDirect
El síndrome de Loeys – Dietz
Vista de Manifestaciones cardiovasculares en el síndrome de Ehlers-Danlos tipo hipermóvil | Revista Peruana de Investigación en Salud
El síndrome de Loeys – Dietz
REDOE - Revista Europea de Odontoestomatologia
Síndrome Aórtico Agudo by FormacionAxarquia FormacionAxarquia - Issuu
PDF) Loeys-Dietz syndrome type 4, caused by chromothripsis, involving the TGFB2 gene
JCM | Free Full-Text | Case-matched Comparison of Cardiovascular Outcome in Loeys-Dietz Syndrome versus Marfan Syndrome
Clinical and radiographic features of the two LDS Patients. A)... | Download Scientific Diagram
Loeys-Dietz and Shprintzen-Goldberg syndromes: analysis of TGF-β-opathies with craniofacial manifestations using an innovative multimodality method | Journal of Medical Genetics
Afectación cardiovascular en el síndrome de Loeys-Dietz | Anales de Pediatría
Frontiers | Identification of a Pathogenic TGFBR2 Variant in a Patient With Loeys–Dietz Syndrome
Neonatal presentation of Loeys-Dietz syndrome: two case reports and review of the literature | Italian Journal of Pediatrics | Full Text
Síndrome de Loeys-Dietz, 3 generaciones, 4 casos familiares
Miguel Marcos on Twitter: "Diagnóstico diferencial de la inflamación de la arteria aorta o aortitis (sí, también puede inflamarse) #FMedUsal #41SEMI" / Twitter
Loeys-Dietz Syndrome Foundation - Care Based Upon Strong Facts 💙 Keep reading to hear from our friend, Dr. Dietz! "I was initially trained as a pediatrician and a cardiologist. I was quite
Study Characterizes Oro-Dental Anomalies in Loeys-Dietz Syndrome
Activation of TGF-β signaling in an aortic aneurysm in a patient with Loeys- Dietz syndrome caused by a novel loss-of-function variant of TGFBR1 | Human Genome Variation
Severity of oro-dental anomalies in Loeys-Dietz syndrome segregates by gene mutation | Journal of Medical Genetics
Oral health-related quality of life in Loeys-Dietz syndrome, a rare connective tissue disorder: an observational cohort study | Orphanet Journal of Rare Diseases | Full Text
Hand and fibrillin‐1 deposition abnormalities in Loeys–Dietz syndrome—expanding the clinical spectrum - Chung - 2014 - American Journal of Medical Genetics Part A - Wiley Online Library
Loeys-Dietz syndrome: MedlinePlus Genetics
