Two Filipino children with oromandibular limb hypogenesis spectrum
Acta Medica Philippina
; : 239-244, 2017.
Article
in English
| WPRIM (Western Pacific)
| ID: wpr-997781
Responsible library:
WPRO
ABSTRACT
@#Oromandibular Limb Hypogenesis Spectrum (OMLHS) [OMIM 103300] is a rare disease characterized by congenital defects of the face, mandible, tongue and hypoplastic limbs. The exact etiology remains unknown. We present two Filipino children diagnosed with OLMHS. Patient 1 is a 2-year-old female noted to have micrognathia, sygnathia and hypoplasia of distal extremities. Patient 2 is a 6-year-old male with hypoplastic mandible, micrognathia, micromelia of both lower extremities and syndactyly of hands. The early recognition of this disease is important so that early surgical correction of deformities particularly the hypoplastic mandible be addressed to avoid complications such as respiratory distress and feeding difficulties.
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Database:
WPRIM (Western Pacific)
Main subject:
Ankyloglossia
Language:
English
Journal:
Acta Medica Philippina
Year:
2017
Document type:
Article