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There are multiple recognized types of RCDP, all of which have autosomal recessive inheritance, and their associated genes are known: RCDP type 1 with <jats:italic>PEX7<\/jats:italic>, RCDP type 2 with <jats:italic>GNPAT<\/jats:italic>, RCDP type 3 with <jats:italic>AGPS<\/jats:italic>, RCDP type 4 with <jats:italic>FAR1<\/jats:italic>, and RCDP type 5 with <jats:italic>PEX5<\/jats:italic>. Among other medical\/developmental issues, plasmalogen deficiency has a direct effect on bone growth and results in postnatal growth failure, the severity of which corresponds to the degree of plasmalogen deficiency. In order to document growth in patients with RCDP, we present detailed growth curves for length, weight, and head circumference derived from retrospective data from 23 individuals with RCDP types 1 and 2 confirmed by molecular and\/or biochemical studies. We stratified growth curves by age as well as by plasmalogen level, with those with higher plasmalogens grouped as \u201cnon\u2010classic.\u201d The growth charts presented here provide guidance to families and physician caretakers on the natural course of growth in individuals with RCDP during infancy into early childhood, and thus will have particular utility in setting expectations and guiding optimal feeding interventions in this population.\u00a9 2016 Wiley Periodicals, Inc.<\/jats:p><\/jats:sec>","DOI":"10.1002\/ajmg.a.37961","type":"journal-article","created":{"date-parts":[[2016,9,12]],"date-time":"2016-09-12T12:08:40Z","timestamp":1473682120000},"page":"108-113","source":"Crossref","is-referenced-by-count":27,"title":["Growth charts for individuals with rhizomelic chondrodysplasia punctata"],"prefix":"10.1002","volume":"173","author":[{"given":"Angela L.","family":"Duker","sequence":"first","affiliation":[{"name":"Division of Medical Genetics Nemours\/Alfred I. duPont Hospital for Children Wilmington Delaware"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tim","family":"Niiler","sequence":"additional","affiliation":[{"name":"Gait Laboratory Nemours\/Alfred I. duPont Hospital for Children Wilmington Delaware"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Grant","family":"Eldridge","sequence":"additional","affiliation":[{"name":"Department of Research Nemours\/Alfred I. duPont Hospital for Children Wilmington Delaware"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nga H.","family":"Brereton","sequence":"additional","affiliation":[{"name":"Institute for Clinical and Translational Research Johns Hopkins School of Medicine Baltimore Maryland"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nancy E.","family":"Braverman","sequence":"additional","affiliation":[{"name":"Departments of Human Genetics and Pediatrics McGill University\u2010Montreal Children's Hospital Research Institute Montreal Quebec"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael B.","family":"Bober","sequence":"additional","affiliation":[{"name":"Division of Medical Genetics Nemours\/Alfred I. duPont Hospital for Children Wilmington Delaware"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"311","published-online":{"date-parts":[[2016,9,12]]},"reference":[{"key":"e_1_2_6_2_1","doi-asserted-by":"publisher","DOI":"10.1186\/1750-1172-8-174"},{"key":"e_1_2_6_3_1","doi-asserted-by":"publisher","DOI":"10.1093\/hmg\/ddv305"},{"key":"e_1_2_6_4_1","doi-asserted-by":"publisher","DOI":"10.1038\/ng0497-369"},{"key":"e_1_2_6_5_1","doi-asserted-by":"publisher","DOI":"10.1002\/humu.10124"},{"key":"e_1_2_6_6_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.bbadis.2012.05.008"},{"key":"e_1_2_6_7_1","unstructured":"BreretonNH RaymondGV MoserAB SnowdenA CarlsonK VogelhutJ.2003. 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