Fine-Lubinsky syndrome: A fourth patient with brachycephaly, deafness, cataract, microstomia and mental retardation

Clinical Dysmorphology

Volumn 5, Issue 1, 1996, Pages 55-60

  Ayme S ^a   Philip, N ^a  

^a INSERM   (France)

Author keywords

Cataract; Craniosynostosis; Deafness; Fine Lubinsky syndrome; Mental retardation; Microstomia

Indexed keywords

ARTICLE; BRACHYCEPHALY; CASE REPORT; CATARACT; CHILD; CRANIOFACIAL SYNOSTOSIS; FEMALE; HEARING IMPAIRMENT; HUMAN; MENTAL RETARDATION MALFORMATION SYNDROME; MICROSTOMIA; PRIORITY JOURNAL; SYNDROME DELINEATION;

ABNORMALITIES, MULTIPLE; CATARACT; DEAFNESS; FEMALE; HUMANS; INFANT, NEWBORN; MENTAL RETARDATION; MICROSTOMIA; SYNDROME;

EID: 0030022508     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-199601000-00008     Document Type: Article

References (3)

1. Fine BE, Lubinsky M (1983): Syndrome identification case report 108: craniofacial and CNS anomalies with body asymmetry, severe retardation, and other malformations. J Clin Dysmorphol 1: 6-9.
2. Preus M, Cooper AR, O'Leary E (1984): Syndrome identification case report 117: sensorineural hearing loss, small facial features, submucous cleft palate, and myoclonic seizures. J Clin Dysmorphol 1: 30-31.
3. Suthers GK, Earley AE, Huson SM (1993): A distinctive syndrome of brachycephaly, deafness, cataracts and mental retardation. Clin Dysmorphol 2: 342-345.