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2.
Genet Couns ; 7(4): 277-82, 1996.
Article in English | MEDLINE | ID: mdl-8985731

ABSTRACT

We report a boy who shows a severe microcephaly, with mild mental retardation and hypotonia, and a dysmorphic facies: (flat profile, arched eyebrows, mild ptosis, short nose with raised basis, large tip and anteverted nares, long, smooth philtrum, narrow mouth with down turned corners, very large, backward tilted ears, with a prominent lobule, retrognathism and very small and widely spaced, although normally shaped teeth. Vesicoureteral reflux was present. The mother showed similar aspect, large ears, and a grinning smile. This appear to represent an undescribed phenotype which share some resemblance to mild Cornelia de Lange and Kabuki syndromes.


Subject(s)
Face/abnormalities , Intellectual Disability/complications , Microcephaly/complications , Adult , Blepharoptosis/complications , Child, Preschool , Female , Humans , Male , Phenotype , Retrognathia/complications , Syndrome
3.
Am J Med Genet ; 43(3): 539-47, 1992 Jun 01.
Article in English | MEDLINE | ID: mdl-1605246

ABSTRACT

Restrictive dermopathy is a rare, lethal autosomal recessive syndrome. We report on 3 unrelated affected stillborn infants of consanguineous parents. Clinical findings include a tight, thin, translucent, taut skin, which tears spontaneously in flexion creases, arthrogryposis multiplex congenita (including the temporomandibular joint), enlarged fontanelles, typical face and dysplasia of clavicles and long bones. Histologic abnormalities include hyperplastic, abnormally keratinized epidermis, reduced tonofilaments, thin, compact dermis with hypoplasia of the elastic fibres, and abnormal subcutaneous fat. Fifteen previous cases are reviewed.


Subject(s)
Abnormalities, Multiple , Arthrogryposis , Bone Diseases, Developmental , Skin Abnormalities , Arthrogryposis/genetics , Biopsy , Bone Diseases, Developmental/diagnostic imaging , Bone Diseases, Developmental/genetics , Face/abnormalities , Female , Humans , Infant, Newborn , Male , Polyhydramnios , Radiography , Syndrome
5.
Clin Genet ; 37(5): 363-6, 1990 May.
Article in English | MEDLINE | ID: mdl-2191794

ABSTRACT

The present report concerns the clinical and cytogenetic findings in a liveborn girl with trisomy for the long arm of chromosome 20. She was the unbalanced product of a maternal t(18;20)(q23.2;q13.1) translocation. Our case is compared to the 3 previous reports of trisomy 20q associated with telomeric translocation. Adenosine deaminase dosage falls in the normal range and confirms the exclusion of the ADA locus from the region extending distally to 20q13.1.


Subject(s)
Chromosomes, Human, Pair 20/ultrastructure , Face/abnormalities , Trisomy , Face/pathology , Female , Humans , Infant , Phenotype
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