Differentials: Multiple Sulfatase Deficiency

Differential diagnosis for Multiple Sulfatase Deficiency

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This list is calculated based on an algorithm and may be inaccurate. Google search based on different algorithm is also displayed. Please interpret with caution. Click here to search for differential diagnosis for a set of clinical findings or a short case summary. The images are provided by Bing Image Search. The images may not be related to Multiple Sulfatase Deficiency.

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Date Added: 2018-03-23:

Multiple Sulfatase Deficiency (100 %) ( Austin Disease, Mucosulfatidosis,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (87 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Harlequin-type Ichthyosis (80 %) ( Harlequin Baby, Harlequin Fetus, Harlequin Ichthyosis, Ichthyosis Congenita, Ichthyosis Congenita Gravior,)
Amniotic Band Syndrome (80 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Aplasia Cutis Congenita (73 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Chondrodysplasia Punctata (73 %)
Cutis Laxa (73 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Joubert Syndrome (73 %)
Rhizomelic Chondrodysplasia Punctata (67 %) ( Autosomal Recessive Chondrodysplasia Punctata Type1, Chondrodystrophia Calcificans Punctata, Peroxisomal Biogenesis Disorder Complementation Group11,)
Phenylketonuria (67 %)
Epidermolytic Hyperkeratosis (67 %) ( Bullous Congenital Ichthyosiform Erythroderma, Bullous Ichthyosiform Erythroderma,)
Mucolipidosis Type Ii (67 %) ( I-cell Disease,)
Collodion Baby (67 %) ( Lamellar Ichthyosis,)
Hyperphenylalaninemia (67 %)
I-cell Disease (67 %) ( Mucolipidosis Type Ii,)
Holocarboxylase Synthetase Deficiency (67 %)
Lamellar Ichthyosis (67 %) ( Collodion Baby,)

Differentials from Google.

Date Added: 2018-04-14

Lipid Storage Disorders
Metachromatic Leukodystrophy
Multiple Sulfatase Deficiency
X-linked Ichthyosis

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I have varied research interests ranging from eHealth, Health Information Exchange, Clinical Trials and Research, Contact Dermatitis, Bioinformatics, and Cosmetic Dermatology. I have work experience in Canada as an eHealth analyst, and in Dubai and India as a Specialist Dermatologist.


Bell Raj Eapen
Hamilton, ON