Differentials: Bloch siemens Syndrome

Differential diagnosis for Bloch siemens Syndrome

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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 Bloch siemens Syndrome.

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Date Added: 2018-02-06:

Incontinentia Pigmenti (100 %) ( Bloch siemens Syndrome, Bloch sulzberger Disease, Bloch sulzberger Syndrome,)
Incontinentia Pigmenti Achromians (40 %) ( Hypomelanosis Of Ito,)
Aplasia Cutis Congenita (40 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Hypomelanosis Of Ito (40 %) ( Incontinentia Pigmenti Achromians,)
Goltz Syndrome (38 %) ( Focal Dermal Hypoplasia,)
Nevus Sebaceous (38 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Focal Dermal Hypoplasia (38 %) ( Goltz Syndrome,)
Nevus Of Ota (38 %) ( Congenital Melanosis Bulbi, Melanosis Bulborum And Aberrant Dermal Melanocytosis, Nevus Fuscoceruleus Ophthalmomaxillaris, Oculodermal Melanocytosis, Oculomucodermal Melanocytosis,)
Hypohidrotic Ectodermal Dysplasia (38 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Nevus Flammeus (36 %) ( Capillary Malformation, Port-wine Stain,)
Cutis Laxa (36 %) ( Chalazoderma, Dermatochalasia, Dermatolysis, Dermatomegaly, Generalized Elastolysis, Generalized Elastorrhexis, Pachydermatocele, Elastolysis,)
Hay wells Syndrome (33 %) ( Aec Syndrome, Ankyloblepharon Filiforme Adnatum ectodermal Dysplasia cleft Palate Syndrome, Ankyloblepharon ectodermal Defects cleft Lip And Palate Syndrome, Ankyloblepharon ectodermal Dysplasia clefting Syndrome,)
Twisted Hairs (33 %) ( Pili Torti,)
Pili Torti (33 %) ( Twisted Hairs,)
Nevus Depigmentosus (33 %) ( Nevus Achromicus,)
Kindler Syndrome (33 %) ( Acrokeratotic Poikiloderma, Bullous Acrokeratotic Poikiloderma Of Kindler And Weary, Congenital Poikiloderma With Blisters And Keratoses, Congenital Poikiloderma With Bullae And Progressive Cutaneous Atrophy, Hereditary Acrokeratotic Poikiloderma, Hyperkeratosis hyperpigmentation Syndrome, Weary kindler Syndrome,)
Nevus Achromicus (33 %) ( Nevus Depigmentosus,)
Dyschromatosis Universalis Hereditaria (31 %)
Eosinophilic Cellulitis (31 %) ( Wells Syndrome,)
Anhidrosis (31 %) ( Hypohidrosis,)
Smooth Tongue (31 %) ( Atrophic Glossitis, Bald Tongue, Hunter Glossitis, Moeller,)
Wells Syndrome (31 %) ( Eosinophilic Cellulitis,)
Tyrosinemia Type Ii (31 %) ( Oculocutaneous Tyrosinemia, Richner hanhart Syndrome,)
Hypohidrosis (31 %) ( Anhidrosis,)
Amniotic Band Syndrome (31 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Waardenburg Syndrome (31 %)
Acrochordon (29 %) ( Cutaneous Papilloma, Cutaneous Tag, Fibroepithelial Polyp, Fibroma Molluscum, Fibroma Pendulum, Papilloma Colli, Skin Tag, Soft Fibroma, Templeton Skin Tag,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (29 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Multiple Lentigines Syndrome (29 %) ( Cardiocutaneous Syndrome, Gorlin Syndrome Ii, Lentiginosis Profusa Syndrome, Leopard Syndrome, Progressive Cardiomyopathic Lentiginosis,)
Juvenile Xanthogranuloma (29 %)
Anetoderma (29 %) ( Anetoderma Maculosa, Anetoderma Maculosa Cutis, Atrophia Maculosa Cutis, Macular Atrophy,)
Postinflammatory Hypermelanosis (29 %) ( Postinflammatory Hyperpigmentation,)
Junctional Epidermolysis Bullosa Gravis (29 %) ( Epidermolysis Bullosa Letalis, Herlitz Disease, Herlitz Epidermolysis Bullosa, Herlitz Syndrome, Lethal Junctional Epidermolysis Bullosa,)
Oculodentodigital Dysplasia (29 %)
Epidermal Nevus Syndrome (29 %) ( Feuerstein And Mims Syndrome, Solomons Syndrome,)
Lichen Striatus (29 %) ( Blaschko Linear Acquired Inflammatory Skin Eruption, Linear Lichenoid Dermatosis,)
Transient Neonatal Pustular Melanosis (29 %) ( Transient Neonatal Pustulosis, Lentigines Neonatorum,)
Telangiectasia (29 %)
Erythema Toxicum Neonatorum (29 %) ( Erythema Toxicum, Toxic Erythema Of The Newborn,)
Postinflammatory Hyperpigmentation (29 %) ( Postinflammatory Hypermelanosis,)
Menkes Kinky Hair Syndrome (29 %) ( Kinky Hair Disease, Menkes Disease,)
Chondrodysplasia Punctata (29 %)

Differentials from Google.

Date Added: 2018-02-17

Epidermal Nevus Syndrome
Incontinentia Pigmenti
Molluscum Contagiosum
Naegeli-franceschetti-jadassohn Syndrome

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Bell Raj Eapen
Hamilton, ON