Placental mesenchymal dysplasia [1]

Pathology

Volumn 34, Issue 4, 2002, Pages 375-378

  Lokan, Julie ^a   Chan, Yuen F ^a   Agnesta, Franca ^a  

^a ROYAL WOMEN'S HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CASE REPORT; FEMALE; HUMAN; LETTER; MESODERM; NEWBORN; PATHOLOGY; PLACENTA; PLACENTA DISORDER; PREGNANCY; PREMATURITY; BECKWITH WIEDEMANN SYNDROME; CLINICAL FEATURE; DYSPLASIA; HISTOPATHOLOGY; HUMAN TISSUE; HYPERINSULINEMIA; HYPOGLYCEMIA; MESENCHYME; NEWBORN DISEASE;

ADULT; FEMALE; HUMANS; INFANT, NEWBORN; INFANT, PREMATURE; MESODERM; PLACENTA; PLACENTA DISEASES; PREGNANCY;

EID: 0036020473     PISSN: 00313025     EISSN: None     Source Type: Journal    
DOI: 10.1080/003130202760120571     Document Type: Article

References (12)

1. Placentomegaly with massive hydrops of placental stem villi, diploid DNA content and fetal omphaloceles: Possible association with Beckwith-Wiedemann syndrome
2. Angiomatous malformation of placental chorionic stem vessels and pseudo partial molar placentas: Report of five cases
3. Ultrasound placental cysts associated with massive placental stem villous hydrops, diploid DNA content, and exomphalos
4. Pregnancy with concomitant chorangioma and placental vascular malformation with mesenchymal hyperplasia
5. Perinatal features associated with placental mesenchymal dysplasia
6. Mesenchymal dysplasia of the placenta
7. Pseudo-partial moles: Placental stem vessel hydrops and the association with Beckwith-Wiedemann syndrome and complete moles
8. Benign hemorrhagic adrenocortical macrocysts in Beckwith-Wiedemann syndrome
9. Hyperinsulinism and Beckwith-Wiedemann syndrome
10. Complete and incomplete forms of Beckwith-Wiedemann syndrome: Their oncogenic potential
11. Incomplete forms of Beckwith-Wiedemann syndrome: Report of a case
12. Molecular genetics of Wiedemann-Beckwith syndrome