Catel-Manzke digitopalatal syndrome or Temtamy preaxial brachydactyly hyperphalangism syndrome? [2]

Clinical Dysmorphology

Volumn 14, Issue 4, 2005, Pages 211-

  Temtamy, Samia A ^a  

^a NATIONAL RESEARCH CENTRE   (Egypt)

Author keywords

Catel Manzke syndrome; New autosomal recessive MCA syndrome; Temtamy preaxial brachydactylyhyperphalangism syndrome

Indexed keywords

AUTOSOMAL RECESSIVE INHERITANCE; BONE MINERALIZATION; BRACHYDACTYLY; CHILD DEVELOPMENT; DENTITION; DIFFERENTIAL DIAGNOSIS; FACIES; FOLLOW UP; FOOT MALFORMATION; GENE MUTATION; HAND MALFORMATION; HUMAN; LETTER; MULTIPLE MALFORMATION SYNDROME; OSTEOPOROSIS; PERCEPTION DEAFNESS; PHENOTYPE; PRIORITY JOURNAL; X RAY;

ABNORMALITIES, MULTIPLE; CHILD, PRESCHOOL; FEMALE; FOLLOW-UP STUDIES; FOOT DEFORMITIES, CONGENITAL; HAND DEFORMITIES, CONGENITAL; HUMANS; INFANT; INFANT, NEWBORN; SYNDROME;

EID: 25844442309     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200510000-00010     Document Type: Letter

References (4)

1. Clarkson JHW, Homfray T, Heron CW, Moss AL (2004). Catel-Manzke syndrome: a case report of a female with severely malformed hands and feet. An extension of the phenotype or a new syndrome? Clin Dysmorphol 13:237-240.
2. OMIM (2005). Online Mendelian Inheritance In Man, Center for Medical Genetics, Johns Hopkins University (Baltimore, M.D.) and the National Center for Biotechnology Information, National Library of Medicine (Bethesda, M.D.). Available from http://www.ncbi.nlm.nih.gov/omim/
3. Temtamy SA, Meguid NA, Ismail SI, Ramzy MI (1998). A new multiple congenital anomaly, mental retardation syndrome with preaxial brachydactyly, hyperphalangism, deafness and orodental anomalies. Clin Dysmorphol 7:249-255.
4. Winter RM, Baraitser M (2001). The London Dysmorphology Data Base: Oxford University Press.