TY - JOUR
T1 - X-Linked Mental Retardation Syndrome
T2 - Three Brothers with the Brooks-Wisniewski-Brown Syndrome
AU - Morava, Éva
AU - Storcz, Judit
AU - Kosztolányi, György
PY - 1996
Y1 - 1996
N2 - We report on 3 brothers with growth and mental retardation, bifrontal narrowness, short palpebral fissures, deeply set eyes with entropion, wide bulbous nose, small mouth, myopia, and spastic diplegia. The patients were born to normal and non-consanguineous parents. The similarity of our cases with those recently reported by Brooks et al. [Am J Med Genet 51:586-590, 1994] supports their suggestion that these patients are representative of a distinct entity.
AB - We report on 3 brothers with growth and mental retardation, bifrontal narrowness, short palpebral fissures, deeply set eyes with entropion, wide bulbous nose, small mouth, myopia, and spastic diplegia. The patients were born to normal and non-consanguineous parents. The similarity of our cases with those recently reported by Brooks et al. [Am J Med Genet 51:586-590, 1994] supports their suggestion that these patients are representative of a distinct entity.
KW - Deeply set eyes
KW - Entropion
KW - New syndrome
KW - Short palpebral fissures
KW - Small mouth
KW - Wide nose tip
KW - X-linked mental retardation
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U2 - 10.1002/(SICI)1096-8628(19960712)64:1<59::AID-AJMG8>3.0.CO;2-M
DO - 10.1002/(SICI)1096-8628(19960712)64:1<59::AID-AJMG8>3.0.CO;2-M
M3 - Article
C2 - 8826449
AN - SCOPUS:0030011778
SN - 0148-7299
VL - 64
SP - 59
EP - 62
JO - American Journal of Medical Genetics - Seminars in Medical Genetics
JF - American Journal of Medical Genetics - Seminars in Medical Genetics
IS - 1
ER -