RESUMO
Clinical and molecular studies are reported on a family with X-linked mental retardation (XLMR) in which there are eight affected males in three generations. Although the males have somatic manifestations, these are variable and in most cases do not allow clear distinction of affected and unaffected males. Affected males are shorter and have a smaller head circumference. Several also have a sloping forehead (5/8), hearing loss (3/8), cupped ears (2/8), and small testes (4/6). An LOD score of 4.41 with zero recombination was obtained at locus DXS1166 in Xq13.2. This family highlights the difficulty in classifying XLMR conditions as either nonsyndromic or syndromic because of the variable somatic manifestations observed in the affected males.
Assuntos
Anormalidades Múltiplas/genética , Deficiência Intelectual/genética , Cromossomo X/genética , Southern Blotting , Mapeamento Cromossômico , DNA/genética , Saúde da Família , Feminino , Ligação Genética , Transtornos do Crescimento , Humanos , Escore Lod , Masculino , Repetições de Microssatélites , Linhagem , Crânio/anormalidades , Testículo/anormalidadesRESUMO
Without an operative Birth Defects Registry, the state of Kentucky does not have a means of determining which of the nearly 6,000 syndromes and birth defects are the most common or the most rare, nor is there an ability to compare and contrast these data with data from other states. The authors reviewed 4,212 charts of patients evaluated between July 1981 and February 1995 by the Division of Genetics and Dysmorphology at the University of Kentucky Chandler Medical Center. Each patient's chart was categorized by diagnosis, and tables were generated to determine the most common diagnoses in the following groups: (1) multiple congenital anomaly syndromes, (2) teratogenic embryopathies, (3) chromosome anomalies, (4) isolated malformations, and (5) bone dysplasias. The most common multiple congenital anomaly syndromes were Down syndrome, Marfan syndrome, and trisomy 18. Fetal alcohol syndrome and infants of diabetic mothers were the most common embryopathies. Spina bifida (meningocele and myelomeningocele) was by far the most common isolated birth defect, followed by cleft lip/ palate and microcephaly. Achondroplasia was the most common bone dysplasia. These data support a number of previous assumptions including the universally high frequency of syndromes like Down syndrome and trisomy 18. The data also give credence to what was previously thought, but unproven, to be a high incidence of diabetic and alcohol embryopathies. The latter (fetal alcohol syndrome) has increased in frequency tremendously over the past 7 years. This is undoubtedly due in part to the overall increased awareness of the diagnosis in the medical community. However, it may also be due to the increased use of alcohol among Kentucky women. Other "rare" disorders, like diastrophic dysplasia, seem to be unusually the diagnosis in the medical community. However, it may also be due to the increased use of alcohol among Kentucky women. Other "rare" disorders, like diastrophic dysplasia, seem to be unusually the diagnosis in the medical community. However, it may also be due to the increased use of alcohol among Kentucky women. Other "rare" disorders, like diastrophic dysplasia, seem to be unusually
Assuntos
Anormalidades Congênitas/epidemiologia , Aberrações Cromossômicas/epidemiologia , Transtornos Cromossômicos , Humanos , Recém-Nascido , Prevalência , SíndromeAssuntos
Testes Genéticos/legislação & jurisprudência , Preconceito , Adulto , Criança , Confidencialidade , Responsabilidade pela Informação , Emprego , Governo Federal , Aconselhamento Genético , Privacidade Genética , Regulamentação Governamental , Humanos , Seguro/legislação & jurisprudência , Seleção Tendenciosa de Seguro , Risco , Governo Estadual , Estados UnidosAssuntos
Cisteína , Variação Genética , Síndrome de Marfan/genética , Proteínas dos Microfilamentos/genética , Sequência de Aminoácidos , Sequência de Bases , Mapeamento Cromossômico , Cromossomos Humanos Par 15 , Primers do DNA , Fator de Crescimento Epidérmico/metabolismo , Fibrilinas , Humanos , Síndrome de Marfan/metabolismo , Proteínas dos Microfilamentos/metabolismo , Dados de Sequência Molecular , Reação em Cadeia da PolimeraseRESUMO
Beare-Stevenson cutis gyrata syndrome consists of skin furrows of corrugated appearance, acanthosis nigricans, craniofacial anomalies, particularly craniosynostosis and ear defects, anogenital anomalies, skin tags, and prominent umbilical stump. Four cases of this striking syndrome are reported. Together with two previously reported cases, the syndrome is delineated from the six known cases. Cutis gyrata variably affects the scalp, forehead, face, preauricular area, neck, trunk, hands, and feet. Craniosynostosis is present in four cases, with cloverleaf skull in three of these. Intrauterine growth has been normal in all cases. Performance and life expectation appear to be related to the presence or absence of cloverleaf skull. All cases observed to date have been sporadic. Increased paternal age suggests the possibility of an autosomal dominant mutation.
Assuntos
Anormalidades Múltiplas/genética , Anormalidades da Pele , Craniossinostoses/genética , Feminino , Humanos , Recém-Nascido , Masculino , Crânio/anormalidades , SíndromeRESUMO
The Marfan syndrome is a common autosomal dominant disorder of connective tissue. Despite many years of intensive investigation, the primary genetic defect has not yet been identified. Reverse genetic methods, targeted at mapping this disease gene, have resulted in an initial report of linkage of the genetic locus for the Marfan phenotype in Finnish families to two polymorphic markers on chromosome 15. We have investigated four large multiplex American families with classic Marfan syndrome using standard genetic linkage methods. Our data confirm the assignment of the Marfan syndrome gene to chromosome 15, but establish a more centromeric location (defined by markers D15S25 and D15S1) as the most probable site for the genetic defect (lod score = 12.1, theta = 0.00). These data should facilitate identification and characterization of the Marfan syndrome gene and, in selected families, have immediate application to diagnosis of equivocal cases or prenatal counseling.
Assuntos
Cromossomos Humanos Par 15 , Ligação Genética , Síndrome de Marfan/genética , Mapeamento Cromossômico , Feminino , Marcadores Genéticos/genética , Genótipo , Humanos , Masculino , Linhagem , FenótipoRESUMO
We are reporting on fifteen members of a five-generation family (sixty-three members) who had an autosomal dominant osseous disorder that was characterized by tarsal and carpal coalition, symphalangism, short first metacarpals, and abnormalities of the elbow, including humeroradial fusion. This family is similar to the one reported by Fuhrmann et al.