Roifman syndrome
- Synonyms
- SPONDYLOEPIPHYSEAL DYSPLASIA, RETINAL DYSTROPHY, AND ANTIBODY DEFICIENCY; Spondyloepiphseal dysplasia, retinal dystrophy and antibody deficiency
- Modes of inheritance
- Autosomal recessive inheritance (Orphanet)
Summary
Excerpted from the GeneReview:- Full text of GeneReview (by section):
- Summary
- GeneReview Scope
- Diagnosis
- Clinical Characteristics
- Genetically Related (Allelic) Disorders
- Differential Diagnosis
- Management
- Genetic Counseling
- Resources
- Molecular Genetics
- Chapter Notes
- References
- Authors:
- Angela Duker
- Danita Velasco
- Nic Robertson
- view full author information
Available tests
Check Related conditions for additional relevant tests.
Clinical features
Help- Abnormality of head or neck
- Anteverted nares
Anteverted nares
- MedGen UID: 326648
- Concept ID: C1840077
- Finding: Finding
Abnormality of head or neck
- Downslanted palpebral fissures
Downslanted palpebral fissures
- MedGen UID: 98391
- Concept ID: C0423110
- Finding: Finding
Abnormality of head or neck
- Downturned corners of mouth
Downturned corners of mouth
- MedGen UID: 356471
- Concept ID: C1866195
- Finding: Anatomical Abnormality
Abnormality of head or neck
- Long palpebral fissure
Long palpebral fissure
- MedGen UID: 340300
- Concept ID: C1849340
- Finding: Finding
Abnormality of head or neck
- Long philtrum
Long philtrum
- MedGen UID: 351278
- Concept ID: C1865014
- Finding: Finding
Abnormality of head or neck
- Narrow nose
Narrow nose
- MedGen UID: 98086
- Concept ID: C0426422
- Finding: Finding
Abnormality of head or neck
- Thin upper lip vermilion
Thin upper lip vermilion
- MedGen UID: 355352
- Concept ID: C1865017
- Finding: Finding
Abnormality of head or neck
- Underdeveloped nasal alae
Underdeveloped nasal alae
- MedGen UID: 322332
- Concept ID: C1834055
- Finding: Congenital Abnormality
Abnormality of head or neck
- Anteverted nares
- Abnormality of limbs
- Brachydactyly
Brachydactyly
- MedGen UID: 67454
- Concept ID: C0221357
- Finding: Congenital Abnormality
Abnormality of limbs
- Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
- MedGen UID: 340456
- Concept ID: C1850049
- Finding: Congenital Abnormality
Abnormality of limbs
- Short digit
Short digit
- MedGen UID: 893063
- Concept ID: C4023124
- Finding: Finding
Abnormality of limbs
- Short metacarpal
Short metacarpal
- MedGen UID: 323064
- Concept ID: C1837084
- Finding: Anatomical Abnormality
Abnormality of limbs
- Short toe
Short toe
- MedGen UID: 322858
- Concept ID: C1836195
- Finding: Finding
Abnormality of limbs
- Single transverse palmar crease
Single transverse palmar crease
- MedGen UID: 96108
- Concept ID: C0424731
- Finding: Finding
Abnormality of limbs
- Brachydactyly
- Abnormality of prenatal development or birth
- Premature birth
Premature birth
- MedGen UID: 57721
- Concept ID: C0151526
- Finding: Pathologic Function
Abnormality of prenatal development or birth
- Premature birth
- Abnormality of the cardiovascular system
- Noncompaction cardiomyopathy
Noncompaction cardiomyopathy
- MedGen UID: 326592
- Concept ID: C1839832
- Finding: Disease or Syndrome
Abnormality of the cardiovascular system
- Ventricular septal defect
Ventricular septal defect
- MedGen UID: 42366
- Concept ID: C0018818
- Finding: Congenital Abnormality
Abnormality of the cardiovascular system
- Noncompaction cardiomyopathy
- Abnormality of the digestive system
- Hepatomegaly
Hepatomegaly
- MedGen UID: 42428
- Concept ID: C0019209
- Finding: Finding
Abnormality of the digestive system
- Hepatomegaly
- Abnormality of the eye
- Retinal dystrophy
Retinal dystrophy
- MedGen UID: 208903
- Concept ID: C0854723
- Finding: Finding
Abnormality of the eye
- Retinal dystrophy
- Abnormality of the immune system
- Eczema
Eczema
- MedGen UID: 3968
- Concept ID: C0013595
- Finding: Disease or Syndrome
Abnormality of the immune system
- Eosinophilia
Eosinophilia
- MedGen UID: 41824
- Concept ID: C0014457
- Finding: Disease or Syndrome
Abnormality of the immune system
- Lymphadenopathy
Lymphadenopathy
- MedGen UID: 96929
- Concept ID: C0497156
- Finding: Disease or Syndrome
Abnormality of the immune system
- Recurrent otitis media
Recurrent otitis media
- MedGen UID: 155436
- Concept ID: C0747085
- Finding: Disease or Syndrome
Abnormality of the immune system
- Splenomegaly
Splenomegaly
- MedGen UID: 52469
- Concept ID: C0038002
- Finding: Finding
Abnormality of the immune system
- Eczema
- Abnormality of the integument
- Prominent eyelashes
Prominent eyelashes
- MedGen UID: 869033
- Concept ID: C4023450
- Finding: Finding
Abnormality of the integument
- Prominent eyelashes
- Abnormality of the musculoskeletal system
- Biconvex vertebral bodies
Biconvex vertebral bodies
- MedGen UID: 355775
- Concept ID: C1866675
- Finding: Finding
Abnormality of the musculoskeletal system
- Generalized hypotonia
Generalized hypotonia
- MedGen UID: 346841
- Concept ID: C1858120
- Finding: Finding
Abnormality of the musculoskeletal system
- Hip contracture
Hip contracture
- MedGen UID: 140815
- Concept ID: C0409354
- Finding: Acquired Abnormality
Abnormality of the musculoskeletal system
- Hypotonia
Hypotonia
- MedGen UID: 10133
- Concept ID: C0026827
- Finding: Finding
Abnormality of the musculoskeletal system
- Irregular femoral epiphysis
Irregular femoral epiphysis
- MedGen UID: 340592
- Concept ID: C1850658
- Finding: Finding
Abnormality of the musculoskeletal system
- Irregular vertebral endplates
Irregular vertebral endplates
- MedGen UID: 331233
- Concept ID: C1842153
- Finding: Finding
Abnormality of the musculoskeletal system
- Microcephaly
Microcephaly
- MedGen UID: 1644158
- Concept ID: C4551563
- Finding: Finding
Abnormality of the musculoskeletal system
- Spondyloepiphyseal dysplasia
Spondyloepiphyseal dysplasia
- MedGen UID: 20916
- Concept ID: C0038015
- Finding: Finding
Abnormality of the musculoskeletal system
- Biconvex vertebral bodies
- Abnormality of the nervous system
- Global developmental delay
Global developmental delay
- MedGen UID: 107838
- Concept ID: C0557874
- Finding: Finding
Abnormality of the nervous system
- Intellectual disability, mild
Intellectual disability, mild
- MedGen UID: 10044
- Concept ID: C0026106
- Finding: Mental or Behavioral Dysfunction
Abnormality of the nervous system
- Global developmental delay
- Abnormality of the respiratory system
- Recurrent pneumonia
Recurrent pneumonia
- MedGen UID: 195802
- Concept ID: C0694550
- Finding: Disease or Syndrome
Abnormality of the respiratory system
- Recurrent pneumonia
- Growth abnormality
- Fetal growth restriction
Fetal growth restriction
- MedGen UID: 4693
- Concept ID: C0015934
- Finding: Pathologic Function
Growth abnormality
- Postnatal growth retardation
Postnatal growth retardation
- MedGen UID: 395343
- Concept ID: C1859778
- Finding: Finding
Growth abnormality
- Short stature
Short stature
- MedGen UID: 87607
- Concept ID: C0349588
- Finding: Finding
Growth abnormality
- Fetal growth restriction
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