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2.
Clin Genet ; 25(6): 500-21, 1984 Jun.
Article in English | MEDLINE | ID: mdl-6539659

ABSTRACT

This is the case report of a patient with Wolf's syndrome having a monosomy 4pter----p15.3 and an additional trisomy 8pter----p22, derived from a maternal balanced translocation t(4;8)(p15.3;p22) after 2:2 disjunction and adjacent-1 segregation. The patient's phenotype is presumably slightly modified by the trisomic 8p segment. Literature analyses indicate that phenotypic "hybrids" with traits of monosomy 4p and of other autosomal segment trisomies exist. The dermatoglyphics of the patient were not highly characteristic for Wolf's syndrome. Also the dermatoglyphics of the balanced translocation carriers were unspecific and did not reflect the carrier status. Pedigree analyses of 46 reported families with reciprocal translocations involving the short arm of chromosome 4 show a high risk (20.5% +/- 4.6%) for unbalanced offspring (trisomy or monosomy 4p) after 2:2 disjunction and adjacent-1 segregation, if the breakpoint in the recipient chromosome is terminal and the resulting imbalance concerns the 4p segment only. It is considerably lower (4.5% +/- 2.5%) if the breakpoint in the recipient chromosome is subterminal, as in the reported case, and the resulting imbalance concerns other chromosome segments additionally to the 4p segment. In both instances, the risk decreases with increasing segment length. The risk for unidentified abortions, stillbirths or neonatal deaths is also high in these families (about 40%). The frequency of progeny with balanced compared to progeny with normal karyotype corresponds to the expected 50% for alternate segregation.


Subject(s)
Chromosome Aberrations/genetics , Chromosome Deletion , Chromosomes, Human, 4-5/ultrastructure , Chromosomes, Human, 6-12 and X/ultrastructure , Diseases in Twins , Translocation, Genetic , Abnormalities, Multiple/genetics , Chromosome Disorders , Dermatoglyphics , Female , Humans , Infant, Newborn , Intellectual Disability/genetics , Male , Pregnancy , Syndrome , Twins, Dizygotic
3.
Hum Genet ; 67(3): 272-95, 1984.
Article in English | MEDLINE | ID: mdl-6469242

ABSTRACT

A photoanthropometric method is presented, which enables an objective definition of facial structures. It may support the clinical description of patients with dysmorphic syndromes. Eighteen parameters were studied. The measuring points were elected on the base of anthropological criteria. The measurements were related to reference values in the same face. The obtained indices were compared to an age related control group of 100 normal children between 0 and 12 years. Values below the 3rd and above the 97th percentile were considered as dysmorphisms. The results give information on the frequency and age dependency of different dysmorphic signs.


Subject(s)
Cephalometry/methods , Face , Age Factors , Child , Child, Preschool , Chromosome Aberrations , Female , Humans , Infant , Infant, Newborn , Male , Maxillofacial Development
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