CYP4F22 gene related symptoms and diseases
All the information presented here about the CYP4F22 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,OMIM,ORPHANET,NCBIGENE, Mendelian Rare Disease Search Engine.
Top 5 symptoms and clinical features associated to CYP4F22 gene
| Symptoms // Phenotype | % Cases |
|---|---|
| Dehydration | Very Common - Between 80% and 100% cases |
| Renal insufficiency | Very Common - Between 80% and 100% cases |
| Hyperkeratosis | Very Common - Between 80% and 100% cases |
| Erythroderma | Very Common - Between 80% and 100% cases |
| Ichthyosis | Very Common - Between 80% and 100% cases |
Other less frequent symptoms and clinical features
Patients with CYP4F22 gene alterations may also develop some of the following symptoms and phenotypes:Commonly - More than 50% cases
- Ectropion
- Sepsis
Not very common - Between 30% and 50% cases
- Short stature
- Nail dystrophy
- Palmoplantar keratoderma
- Epidermal acanthosis
- Absent eyebrow
- Anhidrosis
And 27 more phenotypes, you can get all of them using our tools for rare diseases.
Rare diseases associated to CYP4F22 gene
Here you will find a list of rare diseases related to the CYP4F22. You can also use our tool to get a more accurate diagnosis based on your current symptoms.
LAMELLAR ICHTHYOSIS
Alternate names
LAMELLAR ICHTHYOSIS Is also known as congenital lamellar ichthyosis, li, classic lamellar ichthyosis
Description
Lamellar ichthyosis (LI) is a keratinization disorder characterized by the presence of large scales all over the body without significant erythroderma.
Most common symptoms of LAMELLAR ICHTHYOSIS
- Short stature
- Cognitive impairment
- Abnormality of the dentition
- Renal insufficiency
- Recurrent respiratory infections
More info about LAMELLAR ICHTHYOSIS
SOURCES: ORPHANET
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5; ARCI5
Alternate names
ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5; ARCI5 Is also known as ichthyosis congenita iii, ichthyosis, lamellar, 3, formerly, li3, formerly, nnci, ichthyosis, nonlamellar and nonerythrodermic, congenital, autosomal recessive
Description
Autosomal recessive congenital ichthyosis (ARCI) is a heterogeneous group of disorders of keratinization characterized primarily by abnormal skin scaling over the whole body. These disorders are limited to skin, with approximately two-thirds of patients presenting severe symptoms. The main skin phenotypes are lamellar ichthyosis (LI) and nonbullous congenital ichthyosiform erythroderma (NCIE), although phenotypic overlap within the same patient or among patients from the same family can occur (summary by Fischer, 2009). Neither histopathologic findings nor ultrastructural features clearly distinguish between NCIE and LI. In addition, mutations in several genes have been shown to cause both lamellar and nonbullous ichthyosiform erythrodermal phenotypes (Akiyama et al., 2003). At the First Ichthyosis Consensus Conference in Soreze in 2009, the term 'autosomal recessive congenital ichthyosis' (ARCI) was designated to encompass LI, NCIE, and harlequin ichthyosis (ARCI4B ) (Oji et al., 2010).NCIE is characterized by prominent erythroderma and fine white, superficial, semiadherent scales. Most patients present with collodion membrane at birth and have palmoplantar keratoderma, often with painful fissures, digital contractures, and loss of pulp volume. In half of the cases, a nail dystrophy including ridging, subungual hyperkeratosis, or hypoplasia has been described. Ectropion, eclabium, scalp involvement, and loss of eyebrows and lashes seem to be more frequent in NCIE than in lamellar ichthyosis (summary by Fischer et al., 2000). In LI, the scales are large, adherent, dark, and pigmented with no skin erythema. Overlapping phenotypes may depend on the age of the patient and the region of the body. The terminal differentiation of the epidermis is perturbed in both forms, leading to a reduced barrier function and defects of lipid composition in the stratum corneum (summary by Lefevre et al., 2006).In later life, the skin in ARCI may have scales that cover the entire body surface, including the flexural folds, and the scales are highly variable in size and color. Erythema may be very mild and almost invisible. Some affected persons exhibit scarring alopecia, and many have secondary anhidrosis (summary by Eckl et al., 2005).For a general phenotypic description and discussion of genetic heterogeneity of autosomal recessive congenital ichthyosis, see ARCI1 (OMIM ).
Most common symptoms of ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5; ARCI5
- Flexion contracture
- Renal insufficiency
- Alopecia
- Hyperkeratosis
- Erythema
More info about ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 5; ARCI5
Search interest in CYP4F22
Potential gene panels for CYP4F22 gene
CYP4F22 Panel
Germany.
By Institute for Human Genetics University Clinic Freiburg
This panel specifically test the CYP4F22 gene.
More info about this panel Germany.
CYP4F22. Complete sequencing Panel
Spain.
By Instituto de Medicina Genomica Instituto de Medicina Genomica
This panel specifically test the CYP4F22 gene.
More info about this panel Spain.
Ichthyosis, congenital AR 5 (sequence analysis of CYP4F22 gene) Panel
Portugal.
By CGC Genetics
This panel specifically test the CYP4F22 gene.
More info about this panel Portugal.
Autosomal Recessive Congenital Ichthyosis (ARCI) via CYP4F22 Gene Sequencing with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics
This panel specifically test the CYP4F22 gene.
More info about this panel United States.
Congenital Ichthyosis and Related Disorders Sequencing Panel with CNV Detection Panel
United States.
By PreventionGenetics PreventionGenetics Congenital Ichthyosis and Related Disorders Sequencing Panel with CNV Detection that also includes the following genes: SLC27A4 ST14 TGM1 ALOXE3 ABCA12 CLDN1 POMP PNPLA1 ABHD5 LIPN
More info about this panel United States.
Ichthyosis Deletion / Duplication panel Panel
United States.
By Connective Tissue Gene Tests Ichthyosis Deletion / Duplication panel that also includes the following genes: ST14 STS SULT2B1 TGM1 TGM5 ALOXE3 ABCA12 CASP14 CHST8 CDSN
More info about this panel United States.
Ichthyosis NGS panel Panel
United States.
By Connective Tissue Gene Tests Ichthyosis NGS panel that also includes the following genes: ST14 STS SULT2B1 TGM1 TGM5 ALOXE3 ABCA12 CASP14 CHST8 CDSN
More info about this panel United States.
Ichthyosis Comprehensive panel Panel
United States.
By Connective Tissue Gene Tests Ichthyosis Comprehensive panel that also includes the following genes: ST14 STS SULT2B1 TGM1 TGM5 ALOXE3 ABCA12 CASP14 CHST8 CDSN
More info about this panel United States.
Ichthyosis, lamellar type 3 Panel
Germany.
By Centogene AG - the Rare Disease Company
This panel specifically test the CYP4F22 gene.
More info about this panel Germany.
CentoICU platinum plus Panel
Germany.
By Centogene AG - the Rare Disease Company CentoICU platinum plus that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panel Germany.
New Born testing (CentoICU) Panel
Germany.
By Centogene AG - the Rare Disease Company New Born testing (CentoICU) that also includes the following genes: RMRP BCS1L BDNF RPS19 RPS6KA3 SALL1 SCN1A SCN2A SFTPB SFTPC
More info about this panel Germany.
Ichthyoses and related disorders of cornification Panel Panel
Germany.
By CeGaT GmbH Ichthyoses and related disorders of cornification Panel that also includes the following genes: SLC27A4 SNAP29 ST14 STS TAT TGM1 TGM5 VPS33B ATP2C1 NSDHL
More info about this panel Germany.
ICHTHYOSIS (CONGENITAL) Panel
Spain.
By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases ICHTHYOSIS (CONGENITAL) that also includes the following genes: TGM1 ALOXE3 ABCA12 PNPLA1 CYP4F22 NIPAL4 ALOX12B KRT2
More info about this panel Spain.
CYP4F22 Panel
United States.
By Fulgent Genetics Fulgent Genetics
This panel specifically test the CYP4F22 gene.
More info about this panel United States.
Ichthyosis Panel Panel
Finland.
By Blueprint Genetics Ichthyosis Panel that also includes the following genes: SLC27A4 STS TGM1 ALOXE3 ABCA12 MBTPS2 SPINK5 MPLKIP CDSN SUMF1
More info about this panel Finland.
Congenital lamellar ichthyosis type 5 Panel
Spain.
By Bioarray
This panel specifically test the CYP4F22 gene.
More info about this panel Spain.
ICHTHYOSIS, LAMELLAR , TYPE 3 Panel
Spain.
By Laboratorio de Genetica Clinica SL
This panel specifically test the CYP4F22 gene.
More info about this panel Spain.
ICHTHYOSIS CONGENITA, AUTOSOMAL RECESSIVE: NGS PANEL Panel
Spain.
By Laboratorio de Genetica Clinica SL ICHTHYOSIS CONGENITA, AUTOSOMAL RECESSIVE: NGS PANEL that also includes the following genes: TGM1 ALOXE3 ABCA12 PNPLA1 LIPN CERS3 CYP4F22 NIPAL4 ALOX12B
More info about this panel Spain.
ICHTHYOSIS CONGENITA, AUTOSOMAL RECESSIVE Panel
Spain.
By Laboratorio de Genetica Clinica SL ICHTHYOSIS CONGENITA, AUTOSOMAL RECESSIVE that also includes the following genes: TGM1 ALOXE3 ABCA12 PNPLA1 LIPN CERS3 CYP4F22 NIPAL4 ALOX12B
More info about this panel Spain.
Autosomal Recessive Congenital Ichthyosis Type 5 , Sequencing CYP4F22 Gene Panel
Spain.
By Reference Laboratory Genetics
This panel specifically test the CYP4F22 gene.
More info about this panel Spain.
Congenital Ichthyosis and related disorders , Panel Massive Sequencing (NGS) 33 Genes Panel
Spain.
By Reference Laboratory Genetics Congenital Ichthyosis and related disorders , Panel Massive Sequencing (NGS) 33 Genes that also includes the following genes: SLC27A4 SNAP29 ST14 STS TGM1 TGM5 ALOXE3 ABCA12 SPINK5 MPLKIP
More info about this panel Spain.
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