Gerodermia Osteodysplastica.

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dc.contributor.authorPaul, Rituen_US
dc.contributor.authorKapoor, Seemaen_US
dc.contributor.authorPuri, Ratnaen_US
dc.contributor.authorBijarnia, Sunitaen_US
dc.date.accessioned2004-12-05en_US
dc.date.accessioned2009-05-30T12:52:53Z
dc.date.available2004-12-05en_US
dc.date.available2009-05-30T12:52:53Z
dc.date.issued2004-12-05en_US
dc.description6 references.en_US
dc.description.abstractGerodermia Osteodysplastica is a rare autosomal recessive connective tissue disorder included in the cutis laxa syndromes. Twenty five cases have been reported in the world literature to date. The authors report the first case from our country, a 13 year old female having phenotypic and radiological features suggestive of this genetic disorder.en_US
dc.description.affiliationDepartment of Pediatrics, Maulana Azad Medical College, New Delhi, India.en_US
dc.identifier.citationPaul R, Kapoor S, Puri R, Bijarnia S. Gerodermia Osteodysplastica. Indian Journal of Pediatrics. 2004 Dec; 71(12): e77-79en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/81131
dc.language.isoengen_US
dc.source.urihttps://medind.nic.in/icb/icbai.shtmlen_US
dc.subject.meshAdolescenten_US
dc.subject.meshAging, Premature --diagnosisen_US
dc.subject.meshCutis Laxa --diagnosisen_US
dc.subject.meshFemaleen_US
dc.subject.meshHumansen_US
dc.subject.meshJoint Diseases --diagnosisen_US
dc.subject.meshOsteoporosis --diagnosisen_US
dc.subject.meshPhenotypeen_US
dc.subject.meshSyndromeen_US
dc.titleGerodermia Osteodysplastica.en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
dc.typeReviewen_US
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