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596 Possible Causes for Acroosteolysis

  • Acroosteolysis

    This report described a case of acroosteolysis of phalangeal type associated with regular Down syndrome.[] The authors review the clinical and radiological features of acroosteolysis.[] To demonstrate that severe cold exposure not mounting to frostbite may be associated with acroosteolysis.[]

  • Lytic Bone Lesion

    Acroosteolysis is also linked with several connective tissue diseases.[] Symptoms - Acroosteolysis dominant type Causes - Acroosteolysis dominant type Not supplied. Prevention - Acroosteolysis dominant type Not supplied.[] Diagnostic methods Diagnosis is often delayed due to the relatively late onset of acroosteolysis of distal phalanges.[]

  • Autosomal Recessive Pachydermoperiostosis 

    Guyer PB, Brunton FJ, Wren MW (1978) Pachydermoperiostosis with acroosteolysis. J Bone Joint Surg [Br] 60:219–223 Google Scholar 6.[] The patient was a 37-year-old man with acroosteolysis and digital clubbing of hands and feet fingers and lion facies.[] This is why acroosteolysis and periosteal bone formation can be explained by the action of PGE2.[]

  • Acroosteolysis-Keloid-Like Lesions-Premature Aging Syndrome

    Acroosteolysis is resorption of the distal bony phalanges . Acroosteolysis has two patterns of resorption in adults : diffuse and bandlike.[] Phalangeal acroosteolysis is a rare idiopathic form.[] Zygomatic arch hypoplasia Delayed closure of fontanels Maxillary hypoplasia Thin calvarium - Osteopenia - Delayed bone maturation Spine Scoliosis (in some patients) Hands Acroosteolysis[]

  • Pyknodysostosis

    Differential diagnosis Differential diagnoses include osteoporosis, osteopetrosis, cleidocranial dysplasia and idiopathic acroosteolysis (see these terms).[] Abstract: Patients with pycnodysostosis, a rare skeletal dysplasia, present with bone abnormalities such as short stature, acroosteolysis of distal phalanges, and skull deformities[] Patients with idiopathic acroosteolysis are characterized by hypotelorism, exophthalmos, and an upturned nose.[]

  • Primary Hypergonadotropic Hypogonadism-Partial Alopecia Syndrome

    Syndrome 46,XY Disorder Of Sex Development Due To Isolated 17,20-Lyase Deficiency 46,XY Partial Gonadal Dysgenesis Aarskog-Scott Syndrome Acid-Labile Subunit Deficiency Acroosteolysis[] There is no any evidence of MAD-specific bone dysplasia C) Normal clavicle (D&E) Absent of distal phalange acroosteolysis.[] Mandibuloacral dysplasia with type A lipodystrophy: A disorder characterized by mandibular and clavicular hypoplasia, acroosteolysis, delayed closure of the cranial suture[]

  • Papillon Lefevre Disease

    Subscription Required Diagnostic Pearls Subscription Required Differential Diagnosis & Pitfalls Haim-Munk syndrome comprises palmoplantar keratoderma, arachnodactyly, pes planus, acroosteolysis[] Haim-Munk syndrome shows symptoms such as arachnodactyly, acroosteolysis and onychogryphosis and absent in our patient which lead us to final diagnosis of Papillon Lefevre[] It also exhibits atrophy of nails, arachnodactly, acroosteolysis, and deformity of the phalanges in the hands [ 8 ].[]

  • Acrocephalopolysyndactyly

    Other chapters consider the characteristics of acroosteolysis. This book discusses as well the oral structures in patients with Apert syndrome.[] […] with Osteoporosis and Cha… Acroosteolysis, Giaccai Type Acroosteolysis, Neurogenic ACS ACS I ACS Type III ACS1 ACS3 ACTH Deficiency Actinic Keratosis Active Lifestyle Activity[] Dysostosis, Postaxial Type Acrofacial Dysostosis, Type Genee-Wiedep Acromegaly Acromesomelic Dwarfism Acromesomelic Dysplasia Acromicric Dysplasia Acromicric Skeletal Dysplasia Acroosteolysis[]

  • Autosomal Dominant Hereditary Sensory and Autonomic Neuropathy

    Acroosteolysis, Neurogenic — Acroosteolyses, Neurogenic — Neurogenic Acroosteolyses — Neuropathy, Congenital Sensory — Congenital Sensory Neuropathies — Congenital Sensory[] Sensory Radicular Congenital Insensitivity to Pain with Anhidrosis Congenital Pain Insensitivity with Anhidrosis Congenital Sensory Neuropathy Data Set Dataset Giaccai Type Acroosteolysis[] , Giaccai Type Acroosteolysis, Neurogenic Morvan Disease Neuropathy, Congenital Sensory Neuropathy, Hereditary Sensory Radicular, Autosomal Recessive Neuropathy, Hereditary[]

  • Amaurosis-Hypertrichosis Syndrome

    Causes of Coarse hair Some of the causes of the condition may include: Causes of Coarse Hair : Acrofacial Dysostosis , Catania Type Acroosteolysis Dominant Type Amaurosis-Hypertrichosis[] […] dominant type (Thick eyebrow) Acroosteolysis (Thick eyebrow) Alpha mannosidosis type 2 (Thick eyebrow) ... ...[] […] dominant type Acroosteolysis neurogenic Acroosteolysis osteoporosis skull and mandible changes Acropectoral syndrome Acropectorenal field defect Acropectorovertebral dysplasia[]

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