[Syndromes 2. Pfeiffer syndrome].Ned Tijdschr Tandheelkd. 1998 Jul; 105(7):245-6.NT
Abstract
Acrocephalosyndactylias are syndromes characterized by abnormalities of the head (craniosynostosis), the face (hypertelorism, retromaxillism), hands and feet (cutaneous or bony syndactyly). Inheritance is autosomal dominant, but spontaneous cases are described also. The group is divided into several syndromes with varying penetrance and expressivity. As an example of an acrocephalosyndactylia is the Pfeiffer syndrome presented.
MeSH
Pub Type(s)
English Abstract
Journal Article
Language
dut
PubMed ID
11928428
Citation
Freihofer, H P.. "[Syndromes 2. Pfeiffer Syndrome]." Nederlands Tijdschrift Voor Tandheelkunde, vol. 105, no. 7, 1998, pp. 245-6.
Freihofer HP. [Syndromes 2. Pfeiffer syndrome]. Ned Tijdschr Tandheelkd. 1998;105(7):245-6.
Freihofer, H. P. (1998). [Syndromes 2. Pfeiffer syndrome]. Nederlands Tijdschrift Voor Tandheelkunde, 105(7), 245-6.
Freihofer HP. [Syndromes 2. Pfeiffer Syndrome]. Ned Tijdschr Tandheelkd. 1998;105(7):245-6. PubMed PMID: 11928428.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR
T1 - [Syndromes 2. Pfeiffer syndrome].
A1 - Freihofer,H P,
PY - 2002/4/4/pubmed
PY - 2002/7/26/medline
PY - 2002/4/4/entrez
SP - 245
EP - 6
JF - Nederlands tijdschrift voor tandheelkunde
JO - Ned Tijdschr Tandheelkd
VL - 105
IS - 7
N2 - Acrocephalosyndactylias are syndromes characterized by abnormalities of the head (craniosynostosis), the face (hypertelorism, retromaxillism), hands and feet (cutaneous or bony syndactyly). Inheritance is autosomal dominant, but spontaneous cases are described also. The group is divided into several syndromes with varying penetrance and expressivity. As an example of an acrocephalosyndactylia is the Pfeiffer syndrome presented.
SN - 0028-2200
UR - https://www.unboundmedicine.com/medline/citation/11928428/[Syndromes_2__Pfeiffer_syndrome]_
L2 - https://www.diseaseinfosearch.org/result/5702
DB - PRIME
DP - Unbound Medicine
ER -
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