Familial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings.

scientific article published in January 1984

Familial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1007/BF01601885
P698PubMed publication ID6472918

P2093author name stringG Iannaccone
E Rezza
D Lendvai
P2860cites workCongenital bowing of the long bones. A review and phenotype analysis of 13 undiagnosed casesQ40360079
Heterogeneity in the campomelic syndromes. Long-and short-bone varietiesQ41714151
Familial Congenital Bowing with Short BonesQ41758127
Syndromes of congenital bowing of the long bonesQ44459064
Brief clinical report: skeletal dysplasia with short, angulated femora (kyphomelic dysplasia).Q52282689
Campomelic dysplasia. Further elucidation of a distinct entity.Q52299172
Increasing frequency of a syndrome of multiple osseous defects?Q52331767
Prenatal bowing and thickening of tubular bones, with multiple cutaneous dimples in arms and legs; a congenital syndrome of mechanical origin.Q52370403
Camptomelic dwarfism. A genetically determined mesenchymal disorder combined with sex reversalQ67013316
A variant of campomeliaQ67348959
International nomenclature of constitutional diseases of bone. Revision--May, 1977Q67394509
Sex-reversed XY females with campomelic dysplasia are H-Y negativeQ70666176
Poly-, syn- and oligodactylyl, aplasia or hypoplasia of fibula, hypoplasia of pelvis and bowing of femora in three sibs--a new autosomal recessive syndromeQ71157766
[The campomelic syndrome]Q71786081
P433issue5
P921main subjectsiblingQ31184
P304page(s)323-327
P577publication date1984-01-01
P1433published inPediatric RadiologyQ7159214
P1476titleFamilial congenital bowing with short thick bones and metaphyseal changes, a distinct entity. Report of the clinical and radiological findings in two siblings.
P478volume14