Pfeiffer syndrome, type II

Journal of Perinatology

Volumn 21, Issue 8, 2001, Pages 565-567

  Herman, Thomas E ^a   Siegel, Marilyn J ^a  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ACROCEPHALOSYNDACTYLY; ANORECTAL MALFORMATION; ARTICLE; CASE REPORT; CHILD; CORNEA DISEASE; CRANIOFACIAL SYNOSTOSIS; ECHOGRAPHY; ELBOW DISEASE; EXOPHTHALMOS; EYELID RECONSTRUCTION; FACE DYSMORPHIA; FINGER MALFORMATION; HUMAN; HUMERUS; JOINT CONTRACTURE; KERATOPATHY; KNEE DISEASE; PARITY; RADIOULNAR JOINT; SKULL DEFECT; SPINE MALFORMATION; SYNOSTOSIS;

ACROCEPHALOSYNDACTYLIA; HUMANS; INFANT, NEWBORN;

EID: 0035680862     PISSN: 07438346     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.jp.7210568     Document Type: Article

References (8)

1. Pfeiffer syndrome: Update, clinical subtypes and guidelines for differential diagnosis
2. FGF signaling in skeletal development
3. Evidence for digenic inheritance in some cases of Antley-Bixler syndrome
4. Antley-Bixler syndrome: A disorder characterized by congenital synostosis of the elbow joint and the cranial sature
5. Pfeiffer acrocephalosyndactyly syndrome in mother and son with cloverleaf skull anomaly in the child
6. Hydrocephalus and mental retardation in craniosynostosis
7. Congenital tracheal anomalies in the craniosynostosis syndrome