RT Book, Section A1 Bissonnette, Bruno A1 Luginbuehl, Igor A1 Marciniak, Bruno A1 Dalens, Bernard J. SR Print(0) ID 58066513 T1 Chondrodysplasia Punctata T2 Syndromes: Rapid Recognition and Perioperative Implications YR 2006 FD 2006 PB The McGraw-Hill Companies PP New York, NY SN 9780071354554 LK accessanesthesiology.mhmedical.com/content.aspx?aid=58066513 RD 2024/03/19 AB Refers to a heterogeneous group of disorders having in common ichthyosis and bony abnormalities probably as a result of abnormalities of steroidal biosynthesis. The international nomenclature and classification of osteochondrodysplasias categorized the subtypes of chondrodysplasia punctata as (1) rhizomelic type, (2) Zellweger syndrome, (3) Conradi-Hünermann type, (4) X-linked recessive type, (5) brachytelencephalangic type, (6) tibial-metacarpal type, (7) vitamin K-dependent coagulation defect, and (8) other and acquired genetic disorders including warfarin embryopathy. Specific features of the most common individual types of chondrodysplasia punctata are given below.