Additional case of Keipert syndrome and review of the literature

Medical Science Monitor

Volumn 6, Issue 4, 2000, Pages 776-778

  Cappon, Suzanne M ^a   Khalifa, Mohamed M ^a  

^a QUEEN S UNIVERSITY   (Canada)

Author keywords

Abnormal facies; Broad terminal phalanges; Developmental delay; Sensorineural hearing loss; Syndrome

Indexed keywords

ARTICLE; BEHAVIOR DISORDER; CASE REPORT; CLINICAL FEATURE; FACIES; GENETIC DISORDER; HUMAN; KEIPERT SYNDROME; MALE; MENTAL DEFICIENCY; PERCEPTION DEAFNESS; PSYCHIATRIC TREATMENT; SCHOOL CHILD;

ABNORMALITIES, MULTIPLE; CHILD; DEVELOPMENTAL DISABILITIES; FACE; FOOT DEFORMITIES, CONGENITAL; HAND DEFORMITIES, CONGENITAL; HEARING LOSS, SENSORINEURAL; HUMANS; LINKAGE (GENETICS); MALE; SYNDROME; X CHROMOSOME;

EID: 0033850732     PISSN: 12341010     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (6)

1. A new syndrome of broad terminal phalanges and facial abnormalties
2. Keipert syndrome in two brothers from Turkey
3. Broad thumbs and toes and facial abnormalities
4. A new autosomal recessive syndrome: Peripheral pulmonary stenoses, brachytelephalangism, neural hearing loss and abnormal cartilage calcifications/ossification
5. Familial hand abnormality and sensorineural deafness. A new syndrome
6. Familial broad terminal phalanges with one individual showing additional anomalies