Differentials: Ankyloblepharon ectodermal Dysplasia clefting Syndrome

Differential diagnosis for Ankyloblepharon ectodermal Dysplasia clefting 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 Ankyloblepharon ectodermal Dysplasia clefting Syndrome.

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Date Added: 2018-01-29:

Hay wells Syndrome (100 %) ( Aec Syndrome, Ankyloblepharon Filiforme Adnatum ectodermal Dysplasia cleft Palate Syndrome, Ankyloblepharon ectodermal Defects cleft Lip And Palate Syndrome, Ankyloblepharon ectodermal Dysplasia clefting Syndrome,)
Rapp hodgkin Syndrome (56 %) ( Rapp hodgkin Ectodermal Dysplasia Syndrome,)
Rapp hodgkin Ectodermal Dysplasia Syndrome (56 %) ( Rapp hodgkin Syndrome,)
Aplasia Cutis Congenita (51 %) ( Cutis Aplasia, Congenital Absence Of Skin, Congenital Scars,)
Anhidrosis (51 %) ( Hypohidrosis,)
Hypohidrosis (51 %) ( Anhidrosis,)
Ectodermal Dysplasia (51 %)
Trichorrhexis Invaginata (51 %) ( Bamboo Hair, Netherton Syndrome Or Bamboo Hair,)
Twisted Hairs (49 %) ( Pili Torti,)
Hidrotic Ectodermal Dysplasia (49 %) ( Alopecia Congenita With Keratosis Palmoplantaris, Clouston Syndrome, Cloustons Hidrotic Ectodermal Dysplasia, Fischer jacobsen clouston Syndrome, Keratosis Palmaris With Drumstick Fingers, Palmoplantar Keratoderma And Clubbing,)
Pili Torti (49 %) ( Twisted Hairs,)
Amniotic Band Syndrome (46 %) ( Adam Complex, Amniotic Band Sequence, Congenital Constriction Bands, Pseudoainhum,)
Ectrodactyly ectodermal Dysplasia cleft Syndrome (41 %) ( Eec Syndrome, Split Hand split Foot ectodermal Dysplasia cleft Syndrome,)
Infantile Myofibromatosis (41 %) ( Congenital Generalized Fibromatosis, Congenital Multicentric Fibromatosis,)
Wooly Hair (41 %) ( Woolly Hair,)
Woolly Hair (41 %) ( Wooly Hair,)
Palmoplantar Keratoderma (41 %)
Dystrophic Epidermolysis Bullosa (38 %)
Incontinentia Pigmenti (38 %) ( Bloch siemens Syndrome, Bloch sulzberger Disease, Bloch sulzberger Syndrome,)
Hypohidrotic Ectodermal Dysplasia (38 %) ( Anhidrotic Ectodermal Dysplasia, Christ siemens touraine Syndrome,)
Trichorrhexis Nodosa (38 %)
Ehlers danlos Syndrome (38 %) ( Cutis Hyperelastica, Elastic Skin, India Rubber Skin,)
Hamartoma (36 %)
Kindler Syndrome (36 %) ( 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,)
Lethal Acantholytic Epidermolysis Bullosa (36 %)
Popliteal Pterygium Syndrome (36 %)
Digeorge Syndrome (36 %) ( Digeorge Anomaly, Thymic Hypoplasia,)
Kabuki Syndrome (36 %) ( Kabuki Makeup Syndrome, Niikawa kuroki Syndrome,)
Skin Fragility Syndrome (36 %) ( Plakophilin1 Deficiency,)
Plakophilin1 Deficiency (36 %) ( Skin Fragility Syndrome,)
Nevus Sebaceous (33 %) ( Nevus Sebaceous Of Jadassohn, Organoid Nevus,)
Junctional Epidermolysis Bullosa Gravis (33 %) ( Epidermolysis Bullosa Letalis, Herlitz Disease, Herlitz Epidermolysis Bullosa, Herlitz Syndrome, Lethal Junctional Epidermolysis Bullosa,)
Juvenile Xanthogranuloma (33 %)
Johanson blizzard Syndrome (33 %)
Epidermal Cyst (33 %) ( Epidermal Inclusion Cyst, Epidermoid Cyst, Infundibular Cyst, Keratin Cyst,)
Koilonychia (33 %) ( Spoon Nails,)
Monilethrix (33 %) ( Beaded Hair,)
Ichthyosis brittle Hair impaired Intelligence decreased Fertility short Stature Syndrome (33 %) ( Ibids Syndrome, Sulfur-deficient Brittle Hair Syndrome, Tays Syndrome, Trichothiodystrophy, Trichothiodystrophy With Ichthyosis,)
Dermatopathia Pigmentosa Reticularis (33 %) ( Dermatopathia Pigmentosa Reticularis Hyperkeratotica Et Mutilans, Dermatopathia Pigmentosa Reticularis Hypohidotica Et Atrophica, Dermatopathic Pigmentosa Reticularis,)
Nevus Flammeus (33 %) ( Capillary Malformation, Port-wine Stain,)
Beaded Hair (33 %) ( Monilethrix,)
Familial Cold Autoinflammatory Syndrome (33 %) ( Familial Cold Urticaria,)
Fissured Tongue (33 %) ( Furrowed Tongue, Lingua Plicata, Plicated Tongue, Scrotal Tongue,)
Familial Cold Urticaria (33 %) ( Familial Cold Autoinflammatory Syndrome,)
Follicular Atrophoderma (33 %)
Spoon Nails (33 %) ( Koilonychia,)

Differentials from Google.

From Cache (Web service failed):
Aec Syndrome
Amniotic Band Sequence
Ectodermal Dysplasia
Eec Syndrome
Epidermolysis Bullosa
Epidermolysis Bullosa Simplex
Hidrotic Ectodermal Dysplasia
Hypohidrotic Ectodermal Dysplasia
Wells Syndrome

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