Van der Woude syndrome with sensorineural hearing loss, large craniofacial sinuses, dental pulp stones, and minor limb anomalies: Report of a four-generation Thai family

American Journal of Medical Genetics

Volumn 108, Issue 4, 2002, Pages 275-280

  Kantaputra, Piranit N ^a   Sumitsawan, Yupa ^b   Schutte, Brian C ^c   Tochareontanaphol, Chintana ^d  

^a CHIANG MAI UNIVERSITY   (Thailand)

^b Faculty of Medicine Chiang Mai University   (Thailand)

^c UNIVERSITY OF IOWA   (United States)

^d Chromosome Center   (Thailand)

Author keywords

Brachymesophalangy; Dental anomaly; Large craniofacial sinuses; Lip pit; Pulp stone; Sensorineural hearing loss; Van der Woude syndrome

Indexed keywords

ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CLINICAL FEATURE; CRANIOFACIAL MALFORMATION; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; IMAGE ANALYSIS; LIMB MALFORMATION; MALE; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; THAILAND; TOOTH MALFORMATION; TOOTH PULP DISEASE; VAN DER WOUDE SYNDROME;

ABNORMALITIES, MULTIPLE; ADULT; CHILD; CHILD, PRESCHOOL; CLEFT LIP; CRANIOFACIAL ABNORMALITIES; DENTAL PULP; FAMILY HEALTH; FATAL OUTCOME; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; LIMB DEFORMITIES, CONGENITAL; LIP; MALE; MIDDLE AGED; PEDIGREE; SYNDROME; THAILAND;

EID: 0036531907     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.10276     Document Type: Article

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