Focal dermal hypoplasia (Goltz syndrome).

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dc.contributor.authorRiyaz, Najeebaen_US
dc.contributor.authorRiyaz, Aen_US
dc.contributor.authorChandran, Rajeshen_US
dc.contributor.authorRakesh, S Ven_US
dc.date.accessioned2009-05-28T08:44:52Z
dc.date.available2009-05-28T08:44:52Z
dc.date.issued2005-07-06en_US
dc.description.abstractA 7-year-old girl born of non-consanguineous marriage was evaluated for facial dysmorphism. She had multiple skeletal anomalies like hypoplasia of the right mandible, narrow nasal bridge with broad tip and unilateral notching of the right ala nasi, concomitant squint and low set ears. She also had generalized hypopigmented, atrophic linear macules, multiple papillomas, fat herniations, umbilical hernia, hypoplastic nails, cicatricial alopecia, mild mental retardation, 'lobster-claw' hand and osteopathia striata of long bones, pointing to a diagnosis of Goltz syndrome. The unusual features noted were absence of the left first rib and aortic regurgitation.en_US
dc.description.affiliationDepartments of Dermatology, Medical College, Calicut, Kerala, India. saif_gem@hotmail.comen_US
dc.identifier.citationRiyaz N, Riyaz A, Chandran R, Rakesh SV. Focal dermal hypoplasia (Goltz syndrome). Indian Journal of Dermatology, Venereology and Leprology. 2005 Jul-Aug; 71(4): 279-81en_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/53066
dc.language.isoengen_US
dc.source.urihttps://www.ijdvl.comen_US
dc.subject.meshAbnormalities, Multiple --diagnosisen_US
dc.subject.meshChilden_US
dc.subject.meshFemaleen_US
dc.subject.meshFocal Dermal Hypoplasia --diagnosisen_US
dc.subject.meshFollow-Up Studiesen_US
dc.subject.meshGenetic Predisposition to Diseaseen_US
dc.subject.meshHumansen_US
dc.subject.meshIndiaen_US
dc.subject.meshPedigreeen_US
dc.subject.meshRisk Assessmenten_US
dc.subject.meshSeverity of Illness Indexen_US
dc.titleFocal dermal hypoplasia (Goltz syndrome).en_US
dc.typeCase Reportsen_US
dc.typeJournal Articleen_US
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