3-M syndrome: A prenatal ultrasonographic diagnosis

Prenatal Diagnosis

Volumn 20, Issue 11, 2000, Pages 921-923

  Meo, Francesco ^a,b   Pinto, Vincenzo ^a   D'Addario, Vincenzo ^a  

^a UNIVERSITY OF BARI MEDICAL SCHOOL   (Italy)

^b NONE   (Italy)

Author keywords

Prenatal sonographic diagnosis; Primordial dwarfism; Skeletal dysplasia

Indexed keywords

ADULT; ARTICLE; AUTOPSY; BIRTH WEIGHT; BONE DYSPLASIA; BONE GROWTH; CASE REPORT; CLINICAL FEATURE; DIFFERENTIAL DIAGNOSIS; DISEASE COURSE; DWARFISM; ECHOGRAPHY; FEMALE; GESTATIONAL AGE; HEAD CIRCUMFERENCE; HUMAN; PREGNANCY TERMINATION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL;

EID: 0033653308     PISSN: 01973851     EISSN: None     Source Type: Journal    
DOI: 10.1002/1097-0223(200011)20:11<921::AID-PD947>3.0.CO;2-B     Document Type: Article

References (11)

1. Birth prevalence of skeletal dysplasias in the Italian multicentric monitoring system for birth defects
2. Prenatal diagnosis of asphyxiating thoracic dysplasia (Jeune syndrome)
3. Prenatal ultrasonic diagnosis of a case of Ellis-van Creveld syndrome with a single atrium
4. Case report: Prenatal diagnosis of diastrophic dysplasia by ultrasound at 21 weeks of gestation in a mother with massive obesity
5. In utero analysis of heterozygous achondroplasia: Variable time of onset as detected by femur length measurements
6. Dwarfism with gloomy face: A new feature of 3-M syndrome
7. Bone dysplasia series. Achondroplasia, hypocondroplasia and thanatophoric dysplasia: Review and update
8. The 3-M syndrome: A heritable low birthweight dwarfism
9. Prenatal sonographic diagnosis of type I achondrogenesis with a large hygroma
10. Homozygous achondroplasia: Ultrasonographic distinction between homozygous, heterozygous, and unaffected fetuses in the second trimester
11. Prenatal diagnosis of camptomelic dysplasia