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041 _afre
042 _adc
100 1 0 _aDanarti, Retno
_eauthor
700 1 0 _a Rahmayani, Shinta
_eauthor
700 1 0 _a Wirohadidjojo, Yohanes Widodo
_eauthor
700 1 0 _a Chen, WenChieh
_eauthor
245 0 0 _aDeafness, onychodystrophy, osteodystrophy, mental retardation, and seizures (DOORS) syndrome: a new case report from Indonesia and review of the literature
260 _c2020.
500 _a88
520 _aBackground: DOORS syndrome (deafness, onychodystrophy, osteodystrophy, mental retardation and seizures; MIM 220500) is a rare multisystem genetic disorder, mainly characterized by sensorineural deafness, shortened terminal phalanges with small nails of hands and feet, intellectual deficit, and seizures. The disease is caused by homozygous or compound heterozygous mutation in the TBC1 domain family member 24 (TBC1D24) gene (gene locus/MIM 613577) on chromosome 16p13. Objectives: We report the first case of DOORS syndrome from Indonesia. Materials and Methods: A review of the literature was conducted and cases compared. Results: A 27-day-old baby girl was brought to us with a history of recurrent seizures and absence of all finger- and toenails since birth. In addition, physical examination revealed left eye strabismus and a single transverse palmar crease on both hands. X-rays of the hands and feet showed absence of the distal phalanx of her right and left fingers II-V and the distal phalanx of her right and left toes I-V, respectively. Brainstem-evoked response audiometry test revealed profound bilateral sensorineural deafness. Pentalogy of Fallot was diagnosed by echocardiography, while an abnormal diffuse epileptiform pattern was found on electroencephalography. Conclusion: This is the first report of an association between pentalogy of Fallot and single transverse palmar crease in DOORS syndrome.
690 _apentalogy of Fallot
690 _aTBC1D24
690 _amutation
690 _asingle transverse palmar crease
690 _aDOORS syndrome
690 _aDOOR syndrome
786 0 _nEuropean Journal of Dermatology | 30 | 4 | 2020-07-01 | p. 404-407 | 1167-1122
856 4 1 _uhttps://shs.cairn.info/revue-european-journal-of-dermatology-2020-4-page-404?lang=fr&redirect-ssocas=7080
999 _c602811
_d602811