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A new autosomal dominant craniofacial deafness syndrome.
Clin Genet. 1987 Nov; 32(5):355-9.CG

Abstract

A Jewish family is reported in which the proband and her father had congenital hearing loss and unusual facies consisting of facial asymmetry, temporal alopecia with frontal bossing, a broad nasal root and small nasal alae. In addition, both were born with a short frenulum of the tongue. We believe these findings represent a new autosomal dominant deafness syndrome with distinct craniofacial features.

Authors+Show Affiliations

Department of Medical Genetics, Chaim Sheba Medical Center, Tel-Hashomer, Israel.No affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Case Reports
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

3690878

Citation

Kassutto, S, et al. "A New Autosomal Dominant Craniofacial Deafness Syndrome." Clinical Genetics, vol. 32, no. 5, 1987, pp. 355-9.
Kassutto S, Kassutto Z, Ben-Ami T, et al. A new autosomal dominant craniofacial deafness syndrome. Clin Genet. 1987;32(5):355-9.
Kassutto, S., Kassutto, Z., Ben-Ami, T., & Goodman, R. M. (1987). A new autosomal dominant craniofacial deafness syndrome. Clinical Genetics, 32(5), 355-9.
Kassutto S, et al. A New Autosomal Dominant Craniofacial Deafness Syndrome. Clin Genet. 1987;32(5):355-9. PubMed PMID: 3690878.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - A new autosomal dominant craniofacial deafness syndrome. AU - Kassutto,S, AU - Kassutto,Z, AU - Ben-Ami,T, AU - Goodman,R M, PY - 1987/11/1/pubmed PY - 1987/11/1/medline PY - 1987/11/1/entrez SP - 355 EP - 9 JF - Clinical genetics JO - Clin. Genet. VL - 32 IS - 5 N2 - A Jewish family is reported in which the proband and her father had congenital hearing loss and unusual facies consisting of facial asymmetry, temporal alopecia with frontal bossing, a broad nasal root and small nasal alae. In addition, both were born with a short frenulum of the tongue. We believe these findings represent a new autosomal dominant deafness syndrome with distinct craniofacial features. SN - 0009-9163 UR - https://www.unboundmedicine.com/medline/citation/3690878/A_new_autosomal_dominant_craniofacial_deafness_syndrome_ L2 - https://onlinelibrary.wiley.com/resolve/openurl?genre=article&sid=nlm:pubmed&issn=0009-9163&date=1987&volume=32&issue=5&spage=355 DB - PRIME DP - Unbound Medicine ER -