Literature DB >> 11113897

3-M syndrome: a prenatal ultrasonographic diagnosis.

F Meo1, V Pinto, V D'Addario.   

Abstract

The ultrasonographic imaging of a fetus affected by 3-M syndrome is described. This is a primordial dwarfism with low birthweight, short stature, facial dysmorphism and normal mental development. The biparietal diameter and head circumference were in accordance with the gestational age at 18 weeks. The femur and tibia lengths were on the fifth centile and the radius, ulna and humerus lengths were below the fifth centile. A second scan at 22 weeks showed slowing of growth of all long bones, with the femur, tibia, fibula, humerus, radius and ulna lengths further below the fifth centile. The pregnancy was terminated and postmortem examination confirmed the prenatal diagnosis. The differential diagnosis of skeletal dysplasias characterized by a slow growth of long bones is discussed and the conclusion reached that the detection of shortened long bones (below the fifth centile) is the only ultrasonographic finding of 3-M syndrome. Copyright 2000 John Wiley & Sons, Ltd.

Entities:  

Mesh:

Year:  2000        PMID: 11113897

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


  6 in total

1.  Clinical, molecular and histopathological features of short stature syndrome with novel CUL7 mutation in Yakuts: new population isolate in Asia.

Authors:  N Maksimova; K Hara; A Miyashia; I Nikolaeva; A Shiga; A Nogovicina; A Sukhomyasova; V Argunov; A Shvedova; T Ikeuchi; M Nishizawa; R Kuwano; O Onodera
Journal:  J Med Genet       Date:  2007-08-03       Impact factor: 6.318

2.  Clinical utility gene card for: 3-M syndrome - update 2013.

Authors:  Muriel Holder-Espinasse; Melita Irving; Valérie Cormier-Daire
Journal:  Eur J Hum Genet       Date:  2013-07-31       Impact factor: 4.246

3.  Clinical utility gene card for: 3M syndrome.

Authors:  Muriel Holder-Espinasse; Melita Irving; Valérie Cormier-Daire
Journal:  Eur J Hum Genet       Date:  2011-03-02       Impact factor: 4.246

4.  2D and 3D Ultrasonographic Evaluation of Fetal Midface Hypoplasia in Two Cases with 3-M Syndrome.

Authors:  A Vimercati; A Chincoli; A C de Gennaro; V DʼAddario; E Cicinelli
Journal:  Geburtshilfe Frauenheilkd       Date:  2016-07       Impact factor: 2.915

5.  Neuroblastoma amplified sequence gene is associated with a novel short stature syndrome characterised by optic nerve atrophy and Pelger-Huët anomaly.

Authors:  Nadezda Maksimova; Kenju Hara; Irina Nikolaeva; Tan Chun-Feng; Tomoaki Usui; Mineo Takagi; Yasushi Nishihira; Akinori Miyashita; Hiroshi Fujiwara; Tokuhide Oyama; Anna Nogovicina; Aitalina Sukhomyasova; Svetlana Potapova; Ryozo Kuwano; Hitoshi Takahashi; Masatoyo Nishizawa; Osamu Onodera
Journal:  J Med Genet       Date:  2010-06-24       Impact factor: 6.318

6.  Whole-exome analysis of foetal autopsy tissue reveals a frameshift mutation in OBSL1, consistent with a diagnosis of 3-M Syndrome.

Authors:  Christian R Marshall; Sandra A Farrell; Donna Cushing; Tara Paton; Tracy L Stockley; Dimitri J Stavropoulos; Peter N Ray; Michael Szego; Lynette Lau; Sergio L Pereira; Ronald D Cohn; Richard F Wintle; Adel M Abuzenadah; Muhammad Abu-Elmagd; Stephen W Scherer
Journal:  BMC Genomics       Date:  2015-01-15       Impact factor: 3.969

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.