Literature DB >> 11822087

Association of severe autosomal recessive osteopetrosis and Dandy-Walker syndrome with agenesis of the corpus callosum.

H Ben Hamouda1, M N Sfar, R Braham, M Ben Salah, A Ayadi, H Soua, H Hamza, M T Sfar.   

Abstract

A severe form of autosomal recessive osteopetrosis associated with Dandy-Walker syndrome and agenesis of the corpus callosum is reported in a full-term boy born to consanguineous parents. The diagnosis was made shortly after birth. Clinical features were cranio-facial dysmorphy, macrocephaly, hepatosplenomegaly, severe anemia and thrombocytopenia. Skeletal radiographs revealed generalized increase in bone density and abnormal metaphyseal remodeling. Cranial ultrasonogram and computed tomography scan showed Dandy-Walker syndrome, agenesis of corpus callosum and hydrocephalus. The patient rapidly developed severe medullary deficiency and a severe pulmonary infection. He died at the age of 2 months. This association seems extremely rare and was not previously reported in the literature.

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Year:  2001        PMID: 11822087

Source DB:  PubMed          Journal:  Acta Orthop Belg        ISSN: 0001-6462            Impact factor:   0.500


  6 in total

1.  Endoscopic third ventriculostomy for the treatment of osteopetrosis-related hydrocephalus: a case-based update.

Authors:  Bhoresh Dhamija; Benedetta Ludovica Pettorini; Guirish Solanki
Journal:  Childs Nerv Syst       Date:  2011-05-07       Impact factor: 1.475

2.  New lethal skeletal dysplasia with Dandy-Walker malformation, congenital heart defects, abnormal thumbs, hypoplastic genitalia, and distinctive facies.

Authors:  Cathy A Stevens; Ralph S Lachman
Journal:  Am J Med Genet A       Date:  2010-08       Impact factor: 2.802

Review 3.  Osteopetrosis: genetics, treatment and new insights into osteoclast function.

Authors:  Cristina Sobacchi; Ansgar Schulz; Fraser P Coxon; Anna Villa; Miep H Helfrich
Journal:  Nat Rev Endocrinol       Date:  2013-07-23       Impact factor: 43.330

4.  Anesthesia Management of a Child with Osteopetrosis.

Authors:  Hashem Jarineshin; Fereydoon Fekrat; Mehdi Feiz Dowlat Abadi
Journal:  Anesth Essays Res       Date:  2017 Jul-Sep

5.  SNX10 gene mutation leading to osteopetrosis with dysfunctional osteoclasts.

Authors:  Eva-Lena Stattin; Petra Henning; Joakim Klar; Emma McDermott; Christina Stecksen-Blicks; Per-Erik Sandström; Therese G Kellgren; Patrik Rydén; Göran Hallmans; Torsten Lönnerholm; Adam Ameur; Miep H Helfrich; Fraser P Coxon; Niklas Dahl; Johan Wikström; Ulf H Lerner
Journal:  Sci Rep       Date:  2017-06-07       Impact factor: 4.379

6.  Blake's pouch cyst and Werdnig-Hoffmann disease: Report of a new association and review of the literature.

Authors:  Sherien A Shohoud; Waleed A Azab; Tarek M Alsheikh; Rania M Hegazy
Journal:  Surg Neurol Int       Date:  2014-08-21
  6 in total

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