Abstract |
Adams-Oliver syndrome (AOS) is characterized by the association of scalp and skull defects and abnormalities of terminal limbs. Congenital heart malformations have also been reported. Hepatoportal sclerosis (HPS) is a rare cause of portal hypertension in children characterized by abnormalities of intra-hepatic portal veins, portal fibrosis, and nodular regeneration. Etiopathogenesis of these rare disorders remains unclear, but the hypothesis of vascular thrombotic mechanism has been suggested. Association of both syndromes has been reported in only one child. We now report on two unrelated children with AOS and HPS, one child harboring a factor V Leiden mutation. We hypothesize that the association of both disorders may not be fortuitous and reinforces the idea that AOS and HPS may share a vascular thrombotic mechanism.
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Authors | Muriel Girard, Jeanne Amiel, Monique Fabre, Danièle Pariente, Stanislas Lyonnet, Emmanuel Jacquemin |
Journal | American journal of medical genetics. Part A
(Am J Med Genet A)
Vol. 135
Issue 2
Pg. 186-9
(Jun 01 2005)
ISSN: 1552-4825 [Print] United States |
PMID | 15832360
(Publication Type: Case Reports, Journal Article)
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Copyright | Copyright (c) 2005 Wiley-Liss, Inc. |
Topics |
- Abnormalities, Multiple
(genetics, pathology)
- Child
- Child, Preschool
- Female
- Foot Deformities, Congenital
(pathology)
- Hand Deformities, Congenital
(pathology)
- Humans
- Hypertension, Portal
(pathology)
- Karyotyping
- Limb Deformities, Congenital
(pathology)
- Liver
(blood supply, pathology, physiopathology)
- Male
- Portal Vein
(abnormalities)
- Scalp
(abnormalities)
- Skull
(abnormalities)
- Syndrome
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