TY - JOUR
T1 - The Nance‐Horan syndrome
T2 - a rare X‐linked ocular‐dental trait with expression in heterozygous females
AU - Bixler, David
AU - Higgins, Michael
AU - Hartsfield, James
N1 - Copyright:
Copyright 2016 Elsevier B.V., All rights reserved.
PY - 1984/7
Y1 - 1984/7
N2 - This report describes two families with the Nance‐Horan syndrome, an X‐linked trait featuring lenticular cataracts and anomalies of tooth shape and number. Previous reports have described blindness in affected males but posterior sutural cataracts with normal vision as the primary ocular expression in heterozygous females. In one of these two families, the affected female is not only blind in one eye but reportedly had supernumerary central incisors (mesiodens) removed. This constitutes the most severe ocular and dental expression of this gene in heterozygous females yet reported.
AB - This report describes two families with the Nance‐Horan syndrome, an X‐linked trait featuring lenticular cataracts and anomalies of tooth shape and number. Previous reports have described blindness in affected males but posterior sutural cataracts with normal vision as the primary ocular expression in heterozygous females. In one of these two families, the affected female is not only blind in one eye but reportedly had supernumerary central incisors (mesiodens) removed. This constitutes the most severe ocular and dental expression of this gene in heterozygous females yet reported.
KW - Cataracts
KW - Nance‐Horan syndrome
KW - dental anomalies
KW - heterozygous females
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U2 - 10.1111/j.1399-0004.1984.tb00783.x
DO - 10.1111/j.1399-0004.1984.tb00783.x
M3 - Article
C2 - 6467651
AN - SCOPUS:0021241836
SN - 0009-9163
VL - 26
SP - 30
EP - 35
JO - Clinical Genetics
JF - Clinical Genetics
IS - 1
ER -