Short stature with rhizomelic. Medical search. Frequent questions

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Anatomy7

Microbodies Peroxisomes Fibroblasts Metacarpus Face Facial Bones Chromosomes, Human, X

Diseases36

Chondrodysplasia Punctata, Rhizomelic Chondrodysplasia Punctata Growth Disorders Dwarfism Zellweger Syndrome Refsum Disease Peroxisomal Disorders Turner Syndrome Osteochondrodysplasias Dwarfism, Pituitary Abnormalities, Multiple Noonan Syndrome Bone Diseases, Developmental Syndrome Microcephaly Achondroplasia Puberty, Delayed Intellectual Disability Gonadal Dysgenesis, Mixed Hand Deformities, Congenital Hypertrichosis Laron Syndrome Cephalopelvic Disproportion Puberty, Precocious Dysostoses Failure to Thrive Osteopoikilosis Sex Chromosome Aberrations Cleidocranial Dysplasia Pelger-Huet Anomaly Mental Retardation, X-Linked Lipoid Proteinosis of Urbach and Wiethe Chromosome Disorders Limb Deformities, Congenital Pseudohypoparathyroidism Pigmentation Disorders

Chemicals and Drugs8

Plasmalogens Phytanic Acid Acetyl-CoA C-Acetyltransferase Acyltransferases Human Growth Hormone Receptors, Cytoplasmic and Nuclear Growth Hormone Insulin-Like Growth Factor I

Analytical, Diagnostic and Therapeutic Techniques and Equipment6

Body Height Age Determination by Skeleton Pedigree Growth Charts Karyotyping Anthropometry

Psychiatry and Psychology1

Intellectual Disability

Phenomena and Processes10

Body Height Puberty Consanguinity Phenotype Sex Chromosome Aberrations Genes, Recessive Mutation Bone Development Growth Chromosomes, Human, X

Named Groups1

Infant, Newborn

Health Care1

Anatomy Diseases Chemicals and Drugs Analytical, Diagnostic and Therapeutic Techniques and Equipment Psychiatry and Psychology Phenomena and Processes Named Groups Health Care

Chondrodysplasia Punctata, Rhizomelic Chondrodysplasia Punctata Plasmalogens Growth Disorders Dwarfism Phytanic Acid Zellweger Syndrome Refsum Disease Peroxisomal Disorders Acetyl-CoA C-Acetyltransferase Body Height Turner Syndrome Microbodies Age Determination by Skeleton Osteochondrodysplasias Dwarfism, Pituitary Abnormalities, Multiple Noonan Syndrome Bone Diseases, Developmental Acyltransferases Peroxisomes Syndrome Human Growth Hormone Microcephaly Achondroplasia Puberty, Delayed Receptors, Cytoplasmic and Nuclear Intellectual Disability Gonadal Dysgenesis, Mixed Growth Hormone Fibroblasts Puberty Metacarpus Pedigree Hand Deformities, Congenital Hypertrichosis Laron Syndrome Cephalopelvic Disproportion Consanguinity Growth Charts Puberty, Precocious Dysostoses Phenotype Failure to Thrive Face Facial Bones Osteopoikilosis Sex Chromosome Aberrations Cleidocranial Dysplasia Pelger-Huet Anomaly Genes, Recessive Mutation Mental Retardation, X-Linked Lipoid Proteinosis of Urbach and Wiethe Karyotyping Insulin-Like Growth Factor I Chromosome Disorders Anthropometry Limb Deformities, Congenital Bone Development Growth Infant, Newborn Pseudohypoparathyroidism Chromosomes, Human, X Pigmentation Disorders

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