Keipert syndrome in two brothers from Turkey

Clinical Genetics

Volumn 50, Issue 4, 1996, Pages 223-228

  Balci, Sevim ^a   Dagli, Safak ^b,c  

^a HACETTEPE UNIVERSITY   (Turkey)

^b ANKARA NUMUNE HOSPITAL   (Turkey)

^c VU UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Abnormal facial appearance; Broad terminal phalanges; Keipert syndrome; Pulmonary stenosis; Sensorineural hearing

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; FACIES; FRONTAL BONE; HUMAN; HYPOPLASIA; KEIPERT SYNDROME; MALE; MAXILLA; NOSE MALFORMATION; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PULMONARY VALVE STENOSIS;

EID: 0030457021     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02631.x     Document Type: Article

References (6)

1. Balci S. Two cases of Keipert syndrome from Turkey (broad terminal phalanges, abnormal facies and sensorineural deafness). 18th International Congress of Pediatrics, Philippines, 1983, Abstract of Plenary Sessions and Poster Presentations, vol. 3: 83.
2. Keipert JA, Fitzgerald MG, Danks KM. A new syndrome of broad terminal phalanges and facial abnormalities. Aust Pediatr J 1973: 9: 10-13.
3. Khosroshahi HE, Uluoglu O, Olgunturk R, Basaklar R. Keutel syndrome: a report of four cases. Eur J Pediatr 1989: 149: 188-191.
4. Konigsmark BW, Gorlin RJ. Genetic and metabolic deafness (broad terminal phalanges, abnormal facies and sensorineural deafness). Philadelphia: W.B. Saunders, 1976: 144.
5. Marshall RE, Smith DW. Frontodigital syndrome: a dominantly inherited disorder with normal intelligence. J Pediatr 1970: 77: 129.
6. Rubinstein JH, Taybi H. Broad thumbs and toes an facial abnormalities: a possible mental retardation syndrome. Am J Dis Child 1963: 105: 588.